510(k) K131787 ยท HRN Unit, Cryophthalmic, Ac-Powered
CRYOMATIC MKII CONSOLE, CRYOMATIC MKII PROBES, DISPOSABLE CRYO PROBES
| Applicant | Keeler, Ltd., Broomall PA, US |
| Decision | Substantially Equivalent, Dec 23, 2013 |
| Received | Jun 18, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K131787
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.