510(k) K921988 ยท MDM Instrument, Manual, Surgical, General Use
LACERATION REPAIR TRAY
| Applicant | Cypress Medical Products, Ltd., Mc Henry IL, US |
| Decision | Unknown, Nov 19, 1992 |
| Received | Apr 28, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K921988
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.