REXTAR, REXTAR LCD— 510(k) K122016

Substantially Equivalent

Meta Biomed, Inc.

FDA 510(k) clearance K122016 for REXTAR, REXTAR LCD, Substantially Equivalent on 2013-03-01. Applicant: Meta Biomed, Inc..

Clearance details

Applicant: Meta Biomed, Inc.
Product code: Code EHD
Advisory panel: Dental
Date received: 2012-07-10
Decision date: 2013-03-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mt. Airy, MD, US

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