510(k) K011717 ยท LZA Polymer Patient Examination Glove
SUNMAX BLUE NITRILE POWDERED EXAMINATION GLOVES
| Applicant | Sunmax Enterprise Shanghai Co. , Ltd., Great Neck NY, US |
| Decision | Substantially Equivalent, Aug 14, 2001 |
| Received | Jun 4, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K011717
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.