MEDITRON STETHOSCOPE SYSTEM— 510(k) K991367
Substantially EquivalentMeditron AS
FDA 510(k) clearance K991367 for MEDITRON STETHOSCOPE SYSTEM, Substantially Equivalent on 1999-07-19. Applicant: Meditron AS. Device class: 2.
Clearance details
- Applicant
- Meditron AS
- 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
- Clarksville, MD, US
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