Snyder Laboratories, Inc.: FDA filings under this applicant name
FDA lists 16 510(k) clearances under the applicant name “Snyder Laboratories, Inc.” (first 1978, latest 1984), across 9 product codes in 4 review panels. Median 510(k) review time under this name: 40 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 |
|---|---|---|---|
| GCY | Apparatus, Suction, Single Patient Use, Portable, Nonpowered | 5 | 5 |
| FCM | Tray, Catheterization, Sterile Urethral, With Or Without Catheter (Kit) | 3 | 3 |
| BYY | Tube, Aspirating, Flexible, Connecting | 2 | 2 |
| BSY | Catheters, Suction, Tracheobronchial | 1 | 1 |
| BTA | Pump, Portable, Aspiration (Manual Or Powered) | 1 | 1 |
| EYN | Tray, Irrigation, Sterile | 1 | 1 |
| GBS | Catheter, Ventricular, General & Plastic Surgery | 1 | 1 |
| KDQ | Bottle, Collection, Vacuum | 1 | 1 |
| KNX | Collector, Urine, (And Accessories) For Indwelling Catheter | 1 | 1 |
Review panels
- General and Plastic Surgery (8)
- Gastroenterology and Urology (4)
- General Hospital (3)
- Anesthesiology (1)
Most recent Snyder Laboratories, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K843906 | SNYDER HEMOVAC WOUND DRAINAGE DEVICES | GBS | 1984-11-05 | 33 |
| K821321 | SNYDER DEBRIBEMENT SYSTEM LDP-1 | BTA | 1982-08-06 | 94 |
| K800861 | SNYDER HEMOVAC CHEST DRAINAGE SOLUTION | KDQ | 1980-05-02 | 16 |
| K800578 | SURGIVAC TM | GCY | 1980-04-16 | 33 |
| K800577 | SNYDER HEMOVAC TM VENTED WOUND KIT | GCY | 1980-04-16 | 33 |
| K800543 | SNYDER HYSTERECTOMY Y TUBE KIT | GCY | 1980-04-16 | 37 |
| K800542 | 100 ML SNYDER HEMOVAC | GCY | 1980-04-02 | 23 |
| K790607 | GREENLINE IRRIGATION TRAYS | EYN | 1979-05-11 | 43 |
| K790606 | CATHETERS, GREENLINE SUCTION | BSY | 1979-04-23 | 25 |
| K790420 | SUCTION CONNECTING TUBING | BYY | 1979-04-23 | 54 |
6 earlier clearances. See the full list in Caduvo.
Recalls
openFDA lists no recalls under a recalling firm named Snyder Laboratories, 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.
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.
- Snyder Industries, Inc. (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Snyder Laboratories, Inc.?
FDA lists 16 510(k) clearances under the applicant name “Snyder Laboratories, Inc.” (first 1978, latest 1984), across 9 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 Snyder Laboratories, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Snyder Laboratories, Inc. is 40 days.
Which FDA product codes appear under Snyder Laboratories, Inc.?
The most frequent FDA product codes under this applicant name are GCY (Apparatus, Suction, Single Patient Use, Portable, Nonpowered, 5); FCM (Tray, Catheterization, Sterile Urethral, With Or Without Catheter (Kit), 3); BYY (Tube, Aspirating, Flexible, Connecting, 2).
Next steps
- See all 16 Snyder Laboratories, Inc. clearances with predicates and recalls
- Run predicate analysis for product code GCY, Snyder Laboratories, 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, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.