510(k) K030333 ยท LYY Latex Patient Examination Glove
LATEX EXAMINATION GLOVE,POWEDERED TYPE II, LOW MODULUS,WITH PROTEIN LABLING CLAIM
| Applicant | Perusahaan Getah Asas Sdn. Bhd., Gambrills MD, US |
| Decision | Substantially Equivalent, Mar 21, 2003 |
| Received | Jan 31, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030333
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.