FDA 510(k) Applications for Medical Device Product Code "HEI"
(Monitor, Heart-Valve Movement, Fetal, Ultrasonic)
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K012003 | DOCTOR'S RESEARCH GROUP, INC. | DRG REACTION CHAMBER/SAFETY TIP | 02/12/2002 |
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