510(k) K032940 ยท LYY Latex Patient Examination Glove
BRIGHTWAY BRAND LATEX EXAMINATION GLOVE-(POWDER FREE, STERILE) CONTAINING 50 UGM OR LESS OF WATER EXTRACTABLE PROTEIN PE
| Applicant | Brightway Holdings Sdn. Bhd., Klang, Selangor Darul Ehsan, MY |
| Decision | Substantially Equivalent, Nov 20, 2003 |
| Received | Sep 22, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032940
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.