CKG CARDIOKYMOGRAPH— 510(k) K792051
Substantially EquivalentCardio Kinetics, Inc.
FDA 510(k) clearance K792051 for CKG CARDIOKYMOGRAPH, Substantially Equivalent on 1979-11-13. Applicant: Cardio Kinetics, Inc.. Device class: 2.
Clearance details
- Applicant
- Cardio Kinetics, Inc.
- Product code
- Code DSB
- Device class
- Class 2
- Regulation
- 21 CFR 870.2770
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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