510(k) K863803 ยท JOM Plethysmograph, Photoelectric, Pneumatic Or Hydraulic
VASOPULSE(TM)/MODEL 5000
| Applicant | Sonicaid, Inc., Fredericksburg VA, US |
| Decision | Substantially Equivalent, May 6, 1987 |
| Received | Sep 29, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863803
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.