CRITIKON DUAL CHANNEL RECORDER— 510(k) K792105

Name: FDA 510(k) clearance K792105
Creator: U.S. Food and Drug Administration
Published: 1979-10-26

Substantially Equivalent

Critikon Company, LLC

FDA 510(k) clearance K792105 for CRITIKON DUAL CHANNEL RECORDER, Substantially Equivalent on 1979-10-26. Applicant: Critikon Company, LLC. Device class: 1.

Clearance details

Applicant: Critikon Company, LLC
Product code: Code DSF
Device class: Class 1
Regulation: 21 CFR 870.2810
Advisory panel: Cardiovascular
Date received: 1979-10-22
Decision date: 1979-10-26
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.