SPERTILITE PHOTOTHERAPY LAMP— 510(k) K862608

Name: FDA 510(k) clearance K862608
Creator: U.S. Food and Drug Administration
Published: 1986-08-06

Substantially Equivalent for Some Indications

Cooper-Hewitt Electric Co.

FDA 510(k) clearance K862608 for SPERTILITE PHOTOTHERAPY LAMP, Substantially Equivalent for Some Indications on 1986-08-06. Applicant: Cooper-Hewitt Electric Co.. Device class: 2.

Clearance details

Applicant: Cooper-Hewitt Electric Co.
Product code: Code FTC
Device class: Class 2
Regulation: 21 CFR 878.4630
Advisory panel: General, Plastic Surgery
Date received: 1986-07-08
Decision date: 1986-08-06
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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