FDA 510(k) Applications Submitted by META BIOMED, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K132041 | 07/02/2013 | REXTAR X | META BIOMED, INC. |
| K122016 | 07/10/2012 | REXTAR, REXTAR LCD | META BIOMED, INC. |
| K133298 | 10/25/2013 | ENDO SMART | META BIOMED, INC. |
| K134008 | 12/30/2013 | MD-FLEX HEAVY BODY | META BIOMED, INC. |
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