SKYTRON MODEL 860 AND 800 COMP. SURGITA NEURO EQUI— 510(k) K900472

Name: FDA 510(k) clearance K900472
Creator: U.S. Food and Drug Administration
Published: 1990-09-04

Substantially Equivalent

Skytron, Div. the Kmw Group, Inc.

FDA 510(k) clearance K900472 for SKYTRON MODEL 860 AND 800 COMP. SURGITA NEURO EQUI, Substantially Equivalent on 1990-09-04. Applicant: Skytron, Div. the Kmw Group, Inc.. Device class: 1.

Clearance details

Applicant: Skytron, Div. the Kmw Group, Inc.
Product code: Code HBN
Device class: Class 1
Regulation: 21 CFR 882.4125
Advisory panel: Neurology
Date received: 1990-01-31
Decision date: 1990-09-04
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.