LIFEPAK 5 CARDIOSCOPE-RECORDER MODULE— 510(k) K760676

Name: FDA 510(k) clearance K760676
Creator: U.S. Food and Drug Administration
Published: 1976-10-13

Substantially Equivalent

Physio-Control Corp.

FDA 510(k) clearance K760676 for LIFEPAK 5 CARDIOSCOPE-RECORDER MODULE, Substantially Equivalent on 1976-10-13. Applicant: Physio-Control Corp.. Device class: 1.

Clearance details

Applicant: Physio-Control Corp.
Product code: Code DSF
Device class: Class 1
Regulation: 21 CFR 870.2810
Advisory panel: Cardiovascular
Date received: 1976-09-20
Decision date: 1976-10-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.