Jufrey Multimed Corp.: FDA filings under this applicant name
FDA lists 7 510(k) clearances under the applicant name “Jufrey Multimed Corp.” (first 1985, latest 1986), across 2 product codes in 1 review panel. Median 510(k) review time under this name: 34 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 |
|---|---|---|---|
| FPA | Set, Administration, Intravascular | 6 | 6 |
| BRZ | Set, Blood Transfusion | 1 | 1 |
Review panels
- General Hospital (7)
Most recent Jufrey Multimed Corp. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K861523 | STANDARD BLOOD TRANSFUSION FILTER SET (CODE 1025) | BRZ | 1986-05-27 | 34 |
| K861521 | UNIVERSAL DISPOSABLE INFUSION SET (CODE 0330) | FPA | 1986-05-27 | 34 |
| K861520 | UNIVERSAL DISPOSABLE INFUSION SET (CODE 0205) | FPA | 1986-05-27 | 34 |
| K861519 | UNIVERSAL DISPOSABLE INFUSION SET (CODE 0330F) | FPA | 1986-05-27 | 34 |
| K861518 | UNIVERSAL DISPOSABLE INFUSION SET (CODE 0205F) | FPA | 1986-05-27 | 34 |
| K853527 | JUFREY CORP. UNIV. DISPOS. SCALP VEIN INFUSION SET | FPA | 1985-09-23 | 46 |
| K853327 | JUFREY CORP. UNIVERSAL DISPOS. SCALP VEIN INFUSION | FPA | 1985-08-21 | 13 |
Recalls
openFDA lists no recalls under a recalling firm named Jufrey Multimed 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.
Frequently asked questions
How many FDA 510(k) clearances are listed under Jufrey Multimed Corp.?
FDA lists 7 510(k) clearances under the applicant name “Jufrey Multimed Corp.” (first 1985, latest 1986), across 2 product codes in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Jufrey Multimed Corp.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Jufrey Multimed Corp. is 34 days.
Which FDA product codes appear under Jufrey Multimed Corp.?
The most frequent FDA product codes under this applicant name are FPA (Set, Administration, Intravascular, 6); BRZ (Set, Blood Transfusion, 1).
Next steps
- See all 7 Jufrey Multimed Corp. clearances with predicates and recalls
- Run predicate analysis for product code FPA, Jufrey Multimed 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.