510(k) K961200 ยท EBI Resin, Denture, Relining, Repairing, Rebasing
BOSWORTH LIQUID RESIN II
| Applicant | Harry J. Bosworth Co., Skokie IL, US |
| Decision | Substantially Equivalent, May 17, 1996 |
| Received | Mar 27, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961200
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.