Medical Packaging Corp.: FDA filings under this applicant name
FDA lists 10 510(k) clearances under the applicant name “Medical Packaging Corp.” (first 1987, latest 2001), across 3 product codes in 2 review panels. Median 510(k) review time under this name: 73 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 |
|---|---|---|---|
| JSM | Culture Media, Non-Propagating Transport | 6 | 6 |
| HHT | Spatula, Cervical, Cytological | 2 | 2 |
| LIO | Device, Specimen Collection | 2 | 2 |
Review panels
Most recent Medical Packaging Corp. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K003761 | NAT - NUCLEIC ACID TRANSPORT | LIO | 2001-05-31 | 176 |
| K972726 | SNAP SWAB CULTURE COLLECTION AND TRANSPORT SYSTEM | JSM | 1997-10-08 | 79 |
| K970597 | CULTURE-PAK COLLECTION AND TRANSPORT SYSTEM WITH CLINICAL TRANSPORT MEDIA (CARY-BLAIR OPTION) | JSM | 1997-03-24 | 34 |
| K964637 | CULTURE COLLECTION AND TRANSPORT SYSTEM, MODIFIED AMIES MEDIA | JSM | 1996-12-24 | 35 |
| K936078 | CULTURE-PAK COLLECTION/TRANSPORT SYSTEM, MODIFIED | JSM | 1994-08-16 | 326 |
| K932337 | CULTURE-PAK COLLECTION AND TRANSPORT SYSTEM | JSM | 1994-08-16 | 459 |
| K915454 | CHLAMYDIA TRACHOMATIS SPECIMEN COLLECTION KIT | LIO | 1992-04-08 | 125 |
| K881105 | CULTURE COLLECTION DEVICE | JSM | 1988-04-25 | 41 |
| K870398 | PAP-PAK CYTOBRUSH KIT | HHT | 1987-02-25 | 23 |
| K864323 | CYTOLOGY BRUSHES | HHT | 1987-01-09 | 67 |
Recalls
openFDA lists no recalls under a recalling firm named Medical Packaging Corp..
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.
- Medical Analysis Systems, Inc. (107 510(k)s)
- Medical Components, Inc. (63 510(k)s)
- Medical Advances, Inc. (57 510(k)s)
- Medical Diagnostic Technologies, Inc. (57 510(k)s)
- Medical Devices, Inc. (49 510(k)s)
- Medical Device Technologies, Inc. (46 510(k)s)
- Medical Specialties, Inc. (40 510(k)s)
- Medical Device Inspection Co., Inc. (30 510(k)s)
- Medical Engineering Corp. (28 510(k)s)
- Medical Data Electronics (27 510(k)s)
- Medical Graphics Corp. (25 510(k)s)
- Medical Innovations Corp. (24 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Medical Packaging Corp.?
FDA lists 10 510(k) clearances under the applicant name “Medical Packaging Corp.” (first 1987, latest 2001), across 3 product codes in 2 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 Medical Packaging Corp.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Medical Packaging Corp. is 73 days.
Which FDA product codes appear under Medical Packaging Corp.?
The most frequent FDA product codes under this applicant name are JSM (Culture Media, Non-Propagating Transport, 6); HHT (Spatula, Cervical, Cytological, 2); LIO (Device, Specimen Collection, 2).
Next steps
- See all 10 Medical Packaging Corp. clearances with predicates and recalls
- Run predicate analysis for product code JSM, Medical Packaging Corp.'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.