510(k) K022090 ยท LZA Polymer Patient Examination Glove
SYNTEX PRE-POWDERED NITRILE EXAMINATION GLOVE
| Applicant | Syntex Healthcare Products Co., Ltd., Xinji City, Hebei Province, CN |
| Decision | Substantially Equivalent, Sep 3, 2002 |
| Received | Jun 27, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K022090
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.