510(k) K963365 ยท KMK Device, Intravascular Catheter Securement
MULTI-PURPOSE MEDICAL TUBE HOLDER
| Applicant | Byrd Medical Devices, Inc., Knoxville TN, US |
| Decision | Substantially Equivalent, Oct 11, 1996 |
| Received | Aug 27, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963365
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.