510(k) K954619 ยท KNA Instrument, Manual, Specialized Obstetric-Gynecologic
CORDGUARD II
| Applicant | Utah Medical Products, Inc., Midvale UT, US |
| Decision | Substantially Equivalent, Dec 21, 1995 |
| Received | Oct 5, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954619
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.