510(k) K070760 ยท LYY Latex Patient Examination Glove
POWDER FREE CHLORINATED LATEX PATIENT EXAMINATION GLOVE
| Applicant | Derma Care Plus Products, LLC, Green Bay WI, US |
| Decision | Substantially Equivalent, Jun 7, 2007 |
| Received | Mar 20, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070760
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.