510(k) K950723 ยท DQK Computer, Diagnostic, Programmable
AMBULATORY (HOLTER) RECORDING SYSTEM
| Applicant | Biosensor Corp., Minneapolis MN, US |
| Decision | Substantially Equivalent, Feb 9, 1996 |
| Received | Feb 16, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950723
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.