Redhawk Medical Products & Services, LLC: FDA clearances and approvals
Redhawk Medical Products & Services, LLC has 0 FDA 510(k) clearances, plus 1 PMA decision, across 1 product code in 1 review panel.
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| MTV | Sharps Needle Destruction Device | 1 | 0 |
Review panels
- General Hospital (1)
PMA and De Novo decisions
| Number | Pathway | Device | Decision date |
|---|---|---|---|
| P010040 | PMA | THE DISINTEGRATOR INSULIN NEEDLE DESTRUCTION DEVICE | 2002-03-15 |
Recalls
openFDA lists no recalls under a recalling firm named Redhawk Medical Products & Services, LLC.
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 Redhawk Medical Products & Services, LLC have?
Redhawk Medical Products & Services, LLC has 0 FDA 510(k) clearances, plus 1 PMA decision, across 1 product code in 1 review panel.
What devices does Redhawk Medical Products & Services, LLC make?
Its most frequent FDA product codes are MTV (Sharps Needle Destruction Device, 1).
Has Redhawk Medical Products & Services, LLC had device recalls?
openFDA lists no recalls under a recalling firm name matching Redhawk Medical Products & Services, LLC. Related entities may recall under other names.
Next steps
- See all 0 Redhawk Medical Products & Services, LLC clearances with predicates and recalls
- Run predicate analysis for product code MTV, Redhawk Medical Products & Services, LLC'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.