CADISCOPE ELECTRONIC STETHOSCOPE— 510(k) K990809
Substantially EquivalentCaditec AG
FDA 510(k) clearance K990809 for CADISCOPE ELECTRONIC STETHOSCOPE, Substantially Equivalent on 1999-06-09. Applicant: Caditec AG. Device class: 2.
Clearance details
- Applicant
- Caditec AG
- 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
- Mundelein, IL, US
Recent devices under product code DQD
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