510(k) K050874 ยท GBM Catheter, Urethral
ASTRA TECH AB LOFRIC PRIMO SINGLE USE URINARY CATHETER
| Applicant | Astra Tech, Inc., Northborough MA, US |
| Decision | Substantially Equivalent, May 5, 2005 |
| Received | Apr 6, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K050874
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.