510(k) K842999 ยท KMK Device, Intravascular Catheter Securement
VENI-SHIELD
| Applicant | U.S. Mfg. & Management, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Sep 24, 1984 |
| Received | Jul 30, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K842999
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.