510(k) K010070 ยท MVL Cord, Retraction
ULTRAPAK NEHA
| Applicant | Ultradent Products, Inc., South Jordan UT, US |
| Decision | Substantially Equivalent, Mar 15, 2001 |
| Received | Jan 8, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K010070
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.