510(k) K884362 ยท HQJ Implant, Absorbable, (Scleral Buckling Methods)
LABELING CHANGES TO FYODOROV COLLAGEN CORNEAL SHLD
| Applicant | Bausch & Lomb Pharmaceutical, Inc., Clearwater FL, US |
| Decision | Substantially Equivalent, Nov 29, 1988 |
| Received | Oct 20, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884362
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.