510(k) K971038 ยท DPS Electrocardiograph
KONTRON KOLORMON PLUS ECG WITH RESPIRATION MODULE
| Applicant | Kontron Instruments , Ltd., Watford, Herts, GB |
| Decision | Substantially Equivalent, Sep 24, 1997 |
| Received | Mar 20, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971038
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.