510(k) K012003 ยท HEI Monitor, Heart-Valve Movement, Fetal, Ultrasonic
DRG REACTION CHAMBER/SAFETY TIP
| Applicant | Doctor'S Research Group, Inc., Wolcott CT, US |
| Decision | Substantially Equivalent, Feb 12, 2002 |
| Received | Jun 27, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012003
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.