510(k) K955668 ยท ITX Transducer, Ultrasonic, Diagnostic
INTRACAVITY NEEDLE GUIDE KIT
| Applicant | Arlanda Medicinska Instrument Co. AB, 191 47 Sollentuna, SE |
| Decision | Substantially Equivalent, Jul 30, 1997 |
| Received | Dec 13, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K955668
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.