FDA 510(k) Applications Submitted by ANIARA DIAGNOSTICA ,LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K083729 | 12/16/2008 | HEMOCLOT QUANTI- V-L, FACTOR V-L CALIBRATOR, BIOPHEN V-L CAL (UNDILUTED), BIOPHEN ACT. PC-R CONTROL PLASMA AND BIOPHEN | ANIARA DIAGNOSTICA ,LLC |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact