SERIES 602 CKGTM RECORDER— 510(k) K800851

Substantially Equivalent

Cardio Kinetics, Inc.

FDA 510(k) clearance K800851 for SERIES 602 CKGTM RECORDER, Substantially Equivalent on 1980-04-24. Applicant: Cardio Kinetics, Inc..

Clearance details

Applicant: Cardio Kinetics, Inc.
Product code: Code DSF
Advisory panel: Cardiovascular
Date received: 1980-04-15
Decision date: 1980-04-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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