HALUX TASKLIGHT— 510(k) K931645

Substantially Equivalent

Burton Medical Products Corp.

FDA 510(k) clearance K931645 for HALUX TASKLIGHT, Substantially Equivalent on 1993-08-20. Applicant: Burton Medical Products Corp.. Device class: 1.

Clearance details

Applicant: Burton Medical Products Corp.
Product code: Code KZF
Device class: Class 1
Regulation: 21 CFR 880.6320
Advisory panel: General Hospital
Date received: 1993-04-02
Decision date: 1993-08-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Van Nuys, CA, 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.