SKYTRON EXAM LIGHT— 510(k) K933564

Name: FDA 510(k) clearance K933564
Creator: U.S. Food and Drug Administration
Published: 1994-02-10

Substantially Equivalent

Skytron, Div. the Kmw Group, Inc.

FDA 510(k) clearance K933564 for SKYTRON EXAM LIGHT, Substantially Equivalent on 1994-02-10. Applicant: Skytron, Div. the Kmw Group, Inc.. Device class: 1.

Clearance details

Applicant: Skytron, Div. the Kmw Group, Inc.
Product code: Code KZF
Device class: Class 1
Regulation: 21 CFR 880.6320
Advisory panel: General Hospital
Date received: 1993-07-22
Decision date: 1994-02-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Grand Rapids, MI, 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.