510(k) K970254 ยท MQX Needle, Acupuncture, Single Use
SEIRIN PYONEX ACUPUNCTURE NEEDLES
| Applicant | Seirin-America, Inc., Weymouth MA, US |
| Decision | Substantially Equivalent, Feb 10, 1997 |
| Received | Jan 22, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970254
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.