BETA-CAP II ADAPTER— 510(k) K801680

Substantially Equivalent

Quinton, Inc.

FDA 510(k) clearance K801680 for BETA-CAP II ADAPTER, Substantially Equivalent on 1980-08-04. Applicant: Quinton, Inc.. Device class: 1.

Clearance details

Applicant: Quinton, Inc.
Product code: Code GCE
Device class: Class 1
Regulation: 21 CFR 878.4200
Advisory panel: General, Plastic Surgery
Date received: 1980-07-22
Decision date: 1980-08-04
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.