HAND HELD ATLAS INSTRUMENT— 510(k) K955540

Substantially Equivalent

Spinalight, Inc.

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

Clearance details

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

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