510(k) K830374 ยท KDD Kit, Surgical Instrument, Disposable
RESCUE PACK
| Applicant | Akla, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, May 13, 1983 |
| Received | Feb 4, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830374
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.