510(k) K802557 ยท KDD Kit, Surgical Instrument, Disposable
EMERGENCY DEPARTMENT LACERATION KIT-
| Applicant | Johnson & Johnson Professionals, Inc., Raynham MA, US |
| Decision | Substantially Equivalent, Nov 12, 1980 |
| Received | Oct 16, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802557
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.