510(k) K932300 ยท OCT Anti Fog Solution And Accessories, Endoscopy
FOG CONTROL, LENS FOG REDUCTION DEVICE
| Applicant | Highpoint Medical Corp., Arlington TX, US |
| Decision | Substantially Equivalent, Sep 17, 1993 |
| Received | May 12, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932300
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.