Jufrey Multimed Corp.: FDA clearances and approvals
Jufrey Multimed Corp. has 7 FDA 510(k) clearances (first 1985, latest 1986), across 2 product codes in 1 review panel. Median 510(k) review time: 34 days.
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 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 Jufrey Multimed Corp. have?
Jufrey Multimed Corp. has 7 FDA 510(k) clearances (first 1985, latest 1986), across 2 product codes in 1 review panel.
How long does FDA take to clear Jufrey Multimed Corp.'s 510(k)s?
The median time from FDA receipt to decision across Jufrey Multimed Corp.'s cleared 510(k)s is 34 days.
What devices does Jufrey Multimed Corp. make?
Its most frequent FDA product codes are FPA (Set, Administration, Intravascular, 6); BRZ (Set, Blood Transfusion, 1).
Has Jufrey Multimed Corp. had device recalls?
openFDA lists no recalls under a recalling firm name matching Jufrey Multimed Corp. Related entities may recall under other names.
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. Companies are grouped by FDA applicant name with punctuation and legal suffixes removed. Review days run from FDA receipt to decision. Not regulatory advice.