Multi-Med, Inc.: FDA clearances and approvals
Multi-Med, Inc. has 7 FDA 510(k) clearances (first 1989, latest 1989), across 4 product codes in 2 review panels. Median 510(k) review time: 67 days. openFDA lists 75 product recalls by a recalling firm named Multi-Med, Inc.
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 |
|---|---|---|---|
| FPA | Set, Administration, Intravascular | 3 | 3 |
| FMI | Needle, Hypodermic, Single Lumen | 2 | 2 |
| FPD | Tube, Feeding | 1 | 1 |
| KNT | Tubes, Gastrointestinal (And Accessories) | 1 | 1 |
Review panels
Most recent Multi-Med, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K890424 | ENTERAL FEEDING CONTAINER | KNT | 1989-06-14 | 139 |
| K890396 | EXTERNAL FEEDING SET FOR PUMP USE | FPD | 1989-05-23 | 119 |
| K891176 | INJECTION SITE PLUG (INTRAVASCULAR ADMINISTRATION) | FPA | 1989-05-18 | 73 |
| K891919 | INTRAVASCULAR ADMINISTRATION SET | FMI | 1989-05-05 | 39 |
| K891072 | INTRAVASCULAR ADMINISTRATION SET | FPA | 1989-04-21 | 51 |
| K890340 | INTRAVASCULAR ADMINISTRATION SET | FPA | 1989-03-31 | 67 |
| K890127 | INTRAVASCULAR ADMINISTRATION SET | FMI | 1989-02-03 | 22 |
Recalls
75 product recalls in 2 recall events; 0 initiated in the last five years. Most recent: 2010-08-30.
Recalling firms are matched to this company by name only (same normalization as the applicant), so related entities that recall under another name are not counted.
Frequently asked questions
How many FDA 510(k) clearances does Multi-Med, Inc. have?
Multi-Med, Inc. has 7 FDA 510(k) clearances (first 1989, latest 1989), across 4 product codes in 2 review panels.
How long does FDA take to clear Multi-Med, Inc.'s 510(k)s?
The median time from FDA receipt to decision across Multi-Med, Inc.'s cleared 510(k)s is 67 days.
What devices does Multi-Med, Inc. make?
Its most frequent FDA product codes are FPA (Set, Administration, Intravascular, 3); FMI (Needle, Hypodermic, Single Lumen, 2); FPD (Tube, Feeding, 1).
Has Multi-Med, Inc. had device recalls?
openFDA lists 75 product recalls in 2 recall events by a recalling firm whose name matches Multi-Med, Inc; the most recent began 2010-08-30. Recall firm names are matched by name, so related entities filing under other names are not included.
Next steps
- See all 7 Multi-Med, Inc. clearances with predicates and recalls
- Run predicate analysis for product code FPA, Multi-Med, Inc.'s most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Companies are grouped by FDA applicant name with punctuation and legal suffixes removed. Review days run from FDA receipt to decision. Not regulatory advice.