510(k) K100266 ยท MWJ Electrocardiograph, Ambulatory (Without Analysis)
ACTIWAVE 1E, ACTIWAVE2E, ACTIWAVE2M, ACTIWAVE4E, ACTIWAVE CARDIO MODEL 08-514, 08-521, 08-536, 08-557, 08-603
| Applicant | Camntech, Ltd., Papworth Everard, Cambridgeshire, GB |
| Decision | Substantially Equivalent, Apr 29, 2010 |
| Received | Jan 29, 2010 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K100266
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.