510(k) K973120 ยท GBM Catheter, Urethral
READYCATH CATHETER
| Applicant | Medical Technologies of Georgia, Decatur GA, US |
| Decision | Substantially Equivalent, Feb 25, 1998 |
| Received | Aug 20, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973120
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.