REXTAR X— 510(k) K132041

Substantially Equivalent

Meta Biomed, Inc.

FDA 510(k) clearance K132041 for REXTAR X, Substantially Equivalent on 2013-07-31. Applicant: Meta Biomed, Inc..

Clearance details

Applicant: Meta Biomed, Inc.
Product code: Code EHD
Advisory panel: Dental
Date received: 2013-07-02
Decision date: 2013-07-31
Decision: Substantially Equivalent
Clearance type: Special
Location: Mt. Airy, MD, US

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