510(k) K974561 ยท KYG Device, Irrigation, Ocular Surgery
MOISTAIR FLUID AIR TUBING SET
| Applicant | American Medical Devices, Inc., Atlanta GA, US |
| Decision | Substantially Equivalent, Feb 19, 1998 |
| Received | Dec 5, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K974561
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.