DRG CONVENTIONAL ELECTRONIC DIGITAL STETHOSCOPE, MODEL ECHOP 200-00— 510(k) K991714
Substantially EquivalentDoctor'S Research Group, Inc.
FDA 510(k) clearance K991714 for DRG CONVENTIONAL ELECTRONIC DIGITAL STETHOSCOPE, MODEL ECHOP 200-00, Substantially Equivalent on 1999-12-10. Applicant: Doctor'S Research Group, Inc.. Device class: 2.
Clearance details
- Applicant
- Doctor'S Research Group, Inc.
- Product code
- Code DQD
- Device class
- Class 2
- Regulation
- 21 CFR 870.1875
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Wolcott, CT, US
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