510(k) K923120 ยท GDF Guide, Needle, Surgical
MICROGUIDE LESION MARKING SYSTEM
| Applicant | Angiodynamics, Div. E-Z-Em, Inc., Glens Falls NY, US |
| Decision | Substantially Equivalent, Sep 1, 1992 |
| Received | Jun 26, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K923120
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.