510(k) K972022 ยท FNM Mattress, Air Flotation, Alternating Pressure
ZAK-2000
| Applicant | Cardio Systems, Inc., Carrollton TX, US |
| Decision | Substantially Equivalent, Jan 22, 1998 |
| Received | Jun 2, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972022
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.