CKG CARDIOKYMOGRAPH— 510(k) K792051

Substantially Equivalent

Cardio Kinetics, Inc.

FDA 510(k) clearance K792051 for CKG CARDIOKYMOGRAPH, Substantially Equivalent on 1979-11-13. Applicant: Cardio Kinetics, Inc..

Clearance details

Applicant: Cardio Kinetics, Inc.
Product code: Code DSB
Advisory panel: Cardiovascular
Date received: 1979-10-15
Decision date: 1979-11-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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