510(k) K042099 ยท HKX Tonometer, Ac-Powered
TONOPACH ULTRASONIC TONOMETER/PACHYMETER MODEL P-201 (THE TONOPACH)
| Applicant | Retinapharma Technologies, Inc., Rydal PA, US |
| Decision | Substantially Equivalent, Dec 10, 2004 |
| Received | Aug 4, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K042099
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.