510(k) K003748 ยท MQX Needle, Acupuncture, Single Use
TIANXIE
| Applicant | Suzhou Tianyi Acupuncture Instruments Co., Ltd., Costa Mesa CA, US |
| Decision | Substantially Equivalent, Jan 26, 2001 |
| Received | Dec 4, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K003748
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.