510(k) K101900 ยท GBM Catheter, Urethral
HAKKI URINARY CATHETER; SIZE 14, 16, 18, 20, 22, 24, 26 FRENCH
| Applicant | Hakki Medical Technologies, Inc., Pinellas Park FL, US |
| Decision | Substantially Equivalent, Feb 7, 2011 |
| Received | Jul 7, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101900
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.