510(k) K890182 ยท DSY Prosthesis, Vascular Graft, Of 6mm And Greater Diameter
PROTEGRAFT DV 1500, 1900 & LOW POR, UNIGRAFT DV
| Applicant | Aesculap Instruments Corp., Danville CA, US |
| Decision | Substantially Equivalent, Feb 28, 1990 |
| Received | Jan 18, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890182
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.