510(k) K913696 ยท LDQ
GLOVE-CHEK PORTABLE FLUID LEAKAGE SENSING DEVICE
| Applicant | Vertex Technical Group, Inc., Bethesda MD, US |
| Decision | Substantially Equivalent, Feb 18, 1992 |
| Received | Aug 19, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913696
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.