HAND HELD ATLAS INSTRUMENT— 510(k) K955540

Name: FDA 510(k) clearance K955540
Creator: U.S. Food and Drug Administration
Published: 1996-03-04

Substantially Equivalent

Spinalight, Inc.

FDA 510(k) clearance K955540 for HAND HELD ATLAS INSTRUMENT, Substantially Equivalent on 1996-03-04. Applicant: Spinalight, Inc.. Device class: Unclassified.

Clearance details

Applicant: Spinalight, Inc.
Product code: Code LXM
Device class: Unclassified
Advisory panel: Unknown
Date received: 1995-12-05
Decision date: 1996-03-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Woodstock, GA, US

Download summary PDF View on FDA.gov ↗

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