510(k) K952187 ยท KOB Catheter, Suprapubic (And Accessories)
RUSCH SUPRAFLEX SUPRAPUBIC CYSTOSTOMY CATHETER KIT, STERILE
| Applicant | Rusch, Inc., Jeffrey NH, US |
| Decision | Substantially Equivalent, Jul 25, 1995 |
| Received | May 9, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952187
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.