510(k) K882902 ยท HLR Keratoscope, Battery-Powered
QRK 100, QUALITATIVE RING KERATOSCOPE
| Applicant | Technitex, Inc., Houston TX, US |
| Decision | Substantially Equivalent, Aug 4, 1988 |
| Received | Jul 12, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882902
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.