The following data is part of a premarket notification filed by Doctor's Research Group, Inc. with the FDA for Drg Conventional Electronic Digital Stethoscope, Model Echop 200-00.
Device ID | K991714 |
510k Number | K991714 |
Device Name: | DRG CONVENTIONAL ELECTRONIC DIGITAL STETHOSCOPE, MODEL ECHOP 200-00 |
Classification | Stethoscope, Electronic |
Applicant | DOCTOR'S RESEARCH GROUP, INC. 143 WOLCOTT RD. Wolcott, CT 06716 |
Contact | Richard Deslauriers |
Correspondent | Richard Deslauriers DOCTOR'S RESEARCH GROUP, INC. 143 WOLCOTT RD. Wolcott, CT 06716 |
Product Code | DQD |
CFR Regulation Number | 870.1875 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1999-05-20 |
Decision Date | 1999-12-10 |