510(k) K895431 ยท KMK Device, Intravascular Catheter Securement
JOHNSON & JOHNSON TUBE SECUREMENT DEVICE
| Applicant | Johnson & Johnson Patient Care, Inc., New Brunswick NJ, US |
| Decision | Substantially Equivalent, Oct 13, 1989 |
| Received | Sep 6, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895431
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.