SKYTRON MODEL 610-2— 510(k) K870045

Name: FDA 510(k) clearance K870045
Creator: U.S. Food and Drug Administration
Published: 1987-02-04

Substantially Equivalent

Skytron, Div. the Kmw Group, Inc.

FDA 510(k) clearance K870045 for SKYTRON MODEL 610-2, Substantially Equivalent on 1987-02-04. Applicant: Skytron, Div. the Kmw Group, Inc.. Device class: 2.

Clearance details

Applicant: Skytron, Div. the Kmw Group, Inc.
Product code: Code INX
Device class: Class 2
Regulation: 21 CFR 890.5160
Advisory panel: Physical Medicine
Date received: 1987-01-05
Decision date: 1987-02-04
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.