REXTAR, REXTAR LCD— 510(k) K122016
Substantially EquivalentMeta Biomed, Inc.
FDA 510(k) clearance K122016 for REXTAR, REXTAR LCD, Substantially Equivalent on 2013-03-01. Applicant: Meta Biomed, Inc.. Device class: 2.
Clearance details
- Applicant
- Meta Biomed, Inc.
- Product code
- Code EHD
- Device class
- Class 2
- Regulation
- 21 CFR 872.1800
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mt. Airy, MD, US
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