510(k) K961595 ยท DRL Tester, Defibrillator
DEFIBRILLATOR ANALYZER, DELTA 1000
| Applicant | Netech Corp., Sound Beach NY, US |
| Decision | Substantially Equivalent, Oct 29, 1996 |
| Received | Apr 24, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961595
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.