510(k) K882618 ยท HLR Keratoscope, Battery-Powered
JEDMED/POLACK KERATOSCOPE HS/SL
| Applicant | Gamut Ent., Snellville GA, US |
| Decision | Substantially Equivalent, Jul 13, 1988 |
| Received | Jun 24, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882618
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.