510(k) K881667 ยท GBM Catheter, Urethral
KENDALL CURITY & KENGUARD RED RUBBER URETHRAL CATH
| Applicant | The Kendal Co., Boston MA, US |
| Decision | Substantially Equivalent, Aug 12, 1988 |
| Received | Apr 18, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881667
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.