AMBULATORY ECG DIGITAL MONITOR MODEL: TD-30— 510(k) K880615

Substantially Equivalent

Cardiotechnics, Inc.

FDA 510(k) clearance K880615 for AMBULATORY ECG DIGITAL MONITOR MODEL: TD-30, Substantially Equivalent on 1988-05-13. Applicant: Cardiotechnics, Inc..

Clearance details

Applicant: Cardiotechnics, Inc.
Product code: Code DXH
Advisory panel: Cardiovascular
Date received: 1988-02-16
Decision date: 1988-05-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Big Spring, TX, US

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