SUNFIT SUNLAMP— 510(k) K864485

Substantially Equivalent

Sunfit, Inc.

FDA 510(k) clearance K864485 for SUNFIT SUNLAMP, Substantially Equivalent on 1986-12-17. Applicant: Sunfit, Inc.. Device class: 2.

Clearance details

Applicant: Sunfit, Inc.
Product code: Code FTC
Device class: Class 2
Regulation: 21 CFR 878.4630
Advisory panel: General, Plastic Surgery
Date received: 1986-11-13
Decision date: 1986-12-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New Rochelle, NY, 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.