CADWELL 7200— 510(k) K800648

Substantially Equivalent

Cadwell Laboratories, Inc.

FDA 510(k) clearance K800648 for CADWELL 7200, Substantially Equivalent on 1980-04-21. Applicant: Cadwell Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Cadwell Laboratories, Inc.
Product code: Code IKN
Device class: Class 2
Regulation: 21 CFR 890.1375
Advisory panel: Physical Medicine
Date received: 1980-03-24
Decision date: 1980-04-21
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.