510(k) K992539 ยท LZB Finger Cot
PERCUGUARD
| Applicant | Digit-Pro, Houston TX, US |
| Decision | Substantially Equivalent, Feb 18, 2000 |
| Received | Jul 30, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992539
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.