510(k) K940738 ยท KMF Bandage, Liquid
KTI HY-Q(TM) WOUND DRESSING
| Applicant | Kingston Technologies, Inc., Dayton NJ, US |
| Decision | Substantially Equivalent for Some Indications, May 6, 1994 |
| Received | Feb 17, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K940738
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.