510(k) K970211 ยท DPW Flowmeter, Blood, Cardiovascular
MICROLIFE AUTOMATIC BLOOD PRESSURE MONITOR
| Applicant | Micro Weiss Electronics, Great Neck, NY, US |
| Decision | Substantially Equivalent, Apr 30, 1998 |
| Received | Jan 21, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970211
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.