510(k) K974080 ยท DXQ Blood Pressure Cuff
CRITIKON SOFT BLOOD PRESSURE CUFF
| Applicant | Johnson & Johnson Medical, Inc., Tampa FL, US |
| Decision | Substantially Equivalent, May 18, 1998 |
| Received | Oct 29, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K974080
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Sep 17, 2003 | GE Medical Systems Information Technologies Critikon brand Adult, DURA-CUF, product code 2790, used as an arm cuff in association with a blood pressure monitor. Terminated |
None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.