FDA 510(k) Applications Submitted by METRIKA, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K020234 |
01/23/2002 |
A1CNOW FOR RX HOME USE |
METRIKA, INC. |
| K020235 |
01/23/2002 |
A1CNOW FOR PROFESSIONAL USE |
METRIKA, INC. |
| K033847 |
12/11/2003 |
A1CNOW FOR HOME AND PROFESSIONAL USE |
METRIKA, INC. |
| K051321 |
05/20/2005 |
INVIEW |
METRIKA, INC. |
| K022661 |
08/09/2002 |
A1CNOW FOR HOME USE |
METRIKA, INC. |
| K992997 |
09/07/1999 |
OSTEOMARK NTX POC |
METRIKA, INC. |
| K984530 |
12/21/1998 |
DRX NTX OR, OSTEOMARK NTX DIRECT RESPONSE |
METRIKA, INC. |
| K000887 |
03/20/2000 |
DRX HBA1C |
METRIKA, INC. |
| K000885 |
03/20/2000 |
DRX HBA1C - FOR PRESCRIPTION HOME USE |
METRIKA, INC. |
| K991532 |
05/03/1999 |
DRX QT. HCG |
METRIKA, INC. |
| K991917 |
06/07/1999 |
OSTEOMARK NTX POINT OF CARE (POC) CONTROL SET |
METRIKA, INC. |
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