510(k) K884003 ยท KQX Goniometer, Ac-Powered
GONIOMETER AND BIOMEDICAL RECORDER SYSTEM
| Applicant | Penny & Giles Blackwood , Ltd., England, GB |
| Decision | Substantially Equivalent, Dec 19, 1988 |
| Received | Sep 21, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884003
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.