510(k) K901237 ยท LDQ
GLOVE LEAK DETECTOR
| Applicant | Utah Medical Products, Inc., Midvale UT, US |
| Decision | Substantially Equivalent, Aug 21, 1990 |
| Received | Mar 15, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901237
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.