510(k) K171348 ยท ITX Transducer, Ultrasonic, Diagnostic
Pinpoint GT Needle Guide Kits
| Applicant | C.R. Bard, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, May 22, 2017 |
| Received | May 8, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K171348
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.