510(k) K973362 ยท ITX Transducer, Ultrasonic, Diagnostic
NEEDLE GUIDE/GRID
| Applicant | Protek Medical Products, Inc., Iowa City IA, US |
| Decision | Substantially Equivalent, Oct 1, 1997 |
| Received | Sep 8, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973362
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.