CADWELL 5200— 510(k) K820031

Substantially Equivalent

Cadwell Laboratories, Inc.

FDA 510(k) clearance K820031 for CADWELL 5200, Substantially Equivalent on 1982-02-04. Applicant: Cadwell Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Cadwell Laboratories, Inc.
Product code: Code JXE
Device class: Class 2
Regulation: 21 CFR 882.1550
Advisory panel: Neurology
Date received: 1982-01-06
Decision date: 1982-02-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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