510(k) K781800 ยท KMK Device, Intravascular Catheter Securement
GRIP, HOSPITAL UTILITY
| Applicant | Baka Manufacturing Co., Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 7, 1978 |
| Received | Oct 23, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K781800
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.