510(k) K913941 ยท ITX Transducer, Ultrasonic, Diagnostic
PSG(TM) 20 GUAGE DOPPLER NEEDLE
| Applicant | Peripheral Systems Group, Mountain View CA, US |
| Decision | Substantially Equivalent, Feb 27, 1992 |
| Received | Sep 4, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913941
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.