PSORALITE PHOTOTHERAPY TREATMENT BOOTH, MDL 45000— 510(k) K890084

Name: FDA 510(k) clearance K890084
Creator: U.S. Food and Drug Administration
Published: 1989-05-11

Unknown

Psoralite Corp.

FDA 510(k) clearance K890084 for PSORALITE PHOTOTHERAPY TREATMENT BOOTH, MDL 45000, Unknown on 1989-05-11. Applicant: Psoralite Corp.. Device class: 2.

Clearance details

Applicant: Psoralite Corp.
Product code: Code FTC
Device class: Class 2
Regulation: 21 CFR 878.4630
Advisory panel: General, Plastic Surgery
Date received: 1989-01-10
Decision date: 1989-05-11
Decision: Unknown
Clearance type: Traditional
Location: Columbia, SC, US

Download summary PDF View on FDA.gov ↗

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