510(k) K191705 ยท PGY Display, Diagnostic Radiology
OptikView GUP2103CMI
| Applicant | The Linden Group Corp, Cedar Knolls NJ, US |
| Decision | Substantially Equivalent, Mar 16, 2020 |
| Received | Jun 26, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191705
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.