SUNLAMP— 510(k) K803264

Substantially Equivalent

Am Labs, Inc.

FDA 510(k) clearance K803264 for SUNLAMP, Substantially Equivalent on 1981-06-02. Applicant: Am Labs, Inc..

Clearance details

Applicant: Am Labs, Inc.
Product code: Code FTC
Advisory panel: General, Plastic Surgery
Date received: 1980-12-24
Decision date: 1981-06-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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