510(k) K972525 ยท DRM Compressor, Cardiac, External
THUMPER
| Applicant | Michigan Instruments, Inc., Grand Rapids MI, US |
| Decision | Substantially Equivalent, Oct 2, 1997 |
| Received | Jul 7, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972525
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Feb 13, 2018 | Michigan Instruments, Inc. Thumper Cardiopulmonary Resuscitator, Model 1007CCV, Catalog No. 15370
Product Usage:
The device is used to perform Cardiopulmonary Resuscitation (CRP) on adult patients and only adult patients in cas Terminated |
DRM | None listed |
| Nov 14, 2006 | Michigan Instruments, Inc. Michigan Instruments Thumper Mechanical CPR Device; Model 1007, Part number 15000. Terminated |
DRM | None listed |
| Nov 3, 2006 | Michigan Instruments, Inc. Michigan Instruments Thumper Mechanical CPR Device; Model 1007. Terminated |
DRM | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.