Automatic Liquid Packaging, Inc.: FDA filings under this applicant name
FDA lists 21 510(k) clearances under the applicant name “Automatic Liquid Packaging, Inc.” (first 1983, latest 2000), across 8 product codes in 4 review panels. Median 510(k) review time under this name: 72 days. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.
510(k) clearances per year
| Year | Clearances | Median review days |
|---|---|---|
| 2012 | 0 | — |
| 2013 | 0 | — |
| 2014 | 0 | — |
| 2015 | 0 | — |
| 2016 | 0 | — |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 0 | — |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 0 | — |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| CAF | Nebulizer (Direct Patient Interface) | 7 | 7 |
| BTT | Humidifier, Respiratory Gas, (Direct Patient Interface) | 6 | 6 |
| BTO | Tube, Tracheostomy (W/Wo Connector) | 2 | 2 |
| JOH | Tube Tracheostomy And Tube Cuff | 2 | 2 |
| CCQ | Nebulizer, Medicinal, Non-Ventilatory (Atomizer) | 1 | 1 |
| JOL | Catheter And Tip, Suction | 1 | 1 |
| LPN | Accessories, Soft Lens Products | 1 | 1 |
| LRQ | Tracheostomy And Nasal Suctioning Kit | 1 | 1 |
Review panels
- Anesthesiology (18)
- General Hospital (1)
- Ophthalmic (1)
- General and Plastic Surgery (1)
Most recent Automatic Liquid Packaging, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K994321 | STERILE WATER AND 0.9% SODIUM CHLORIDE FOR IRRIGATION, USP | JOL | 2000-10-25 | 308 |
| K000964 | STERILE WATER OR O.9% SODIUM CHLORIDE, MODEL AL4100 & AL4109 | JOH | 2000-04-25 | 29 |
| K980147 | YOUR CHOICE MULTI-PURPOSE CONTACT LENS CLEANING SOLUTION | LPN | 1998-04-13 | 88 |
| K973829 | IRRIGATION BOTTLE | JOH | 1998-02-23 | 139 |
| K962079 | HUMIDIFIER ADAPTER | BTT | 1996-07-31 | 64 |
| K955104 | HIGH FLOW ADJUSTABLE ENTRAINMENT NEBULIZER | CAF | 1996-06-11 | 216 |
| K920306 | OPTI-MOL FILTERED PUNCTURE PIN | BTT | 1992-04-06 | 75 |
| K911770 | OPTIMOL RESPIRATORY HUMIDIFICATION SYSTEM | BTT | 1991-10-15 | 179 |
| K901762 | PREFILLED FLEXIBLE R.T. CONTAINERS W/STER. SODIUM | BTT | 1990-07-17 | 90 |
| K901362 | ACCESSORY FITMENT TO NEBULIZER SYSTEM, STERILE | CAF | 1990-06-06 | 75 |
11 earlier clearances. See the full list in Caduvo.
Recalls
openFDA lists no recalls under a recalling firm named Automatic Liquid Packaging, Inc..
Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.
Related HCPCS codes
HCPCS Level II codes whose descriptors match the device names of the product codes filed under Automatic Liquid Packaging, Inc. (a text match, not an official crosswalk):
Other FDA applicant names starting with the same word
FDA records these as separate applicants. Some may belong to the same corporate group and some may not; their filings are not included in the counts above.
- Automatic Medical Technologies, Inc. (2 510(k)s)
- Automatic Film Processor Corp. (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Automatic Liquid Packaging, Inc.?
FDA lists 21 510(k) clearances under the applicant name “Automatic Liquid Packaging, Inc.” (first 1983, latest 2000), across 8 product codes in 4 review panels. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Automatic Liquid Packaging, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Automatic Liquid Packaging, Inc. is 72 days.
Which FDA product codes appear under Automatic Liquid Packaging, Inc.?
The most frequent FDA product codes under this applicant name are CAF (Nebulizer (Direct Patient Interface), 7); BTT (Humidifier, Respiratory Gas, (Direct Patient Interface), 6); BTO (Tube, Tracheostomy (W/Wo Connector), 2).
Next steps
- See all 21 Automatic Liquid Packaging, Inc. clearances with predicates and recalls
- Run predicate analysis for product code CAF, Automatic Liquid Packaging, Inc.'s most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name (spelling variants such as punctuation and legal suffixes combined); filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.