510(k) K962327 ยท FMQ Restraint, Protective
SEKURE SEAT ADULT PASSIVE RESTRAINING DEVICE
| Applicant | Sekure Seat Corp., Hickory NC, US |
| Decision | Substantially Equivalent, Mar 6, 1997 |
| Received | Jun 17, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962327
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.