Metrika, Inc. is one of 25989 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Metrika, Inc. - FDA 510(k) Cleared Devices
Recent clearances: INVIEW, A1CNOW FOR HOME AND PROFESSIONAL USE, A1CNOW FOR HOME USE
11
Total
11
Cleared
0
Denied
Metrika, Inc. has 11 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.
Historical record: 11 cleared submissions from 1999 to 2005. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Metrika, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Metrika, Inc.
11 devices
Cleared
Jun 13, 2005
INVIEW
Chemistry
24d
Cleared
Dec 23, 2003
A1CNOW FOR HOME AND PROFESSIONAL USE
Chemistry
12d
Cleared
Dec 13, 2002
A1CNOW FOR HOME USE
Hematology
126d
Cleared
Feb 15, 2002
A1CNOW FOR RX HOME USE
Hematology
23d
Cleared
Feb 15, 2002
A1CNOW FOR PROFESSIONAL USE
Hematology
23d
Cleared
Sep 26, 2000
DRX HBA1C - FOR PRESCRIPTION HOME USE
Hematology
190d
Cleared
Jul 26, 2000
DRX HBA1C
Hematology
128d
Cleared
Nov 09, 1999
OSTEOMARK NTX POC
Chemistry
63d
Cleared
Sep 17, 1999
DRX QT. HCG
Chemistry
137d
Cleared
Aug 10, 1999
DRX NTX OR, OSTEOMARK NTX DIRECT RESPONSE
Chemistry
232d
Cleared
Jul 12, 1999
OSTEOMARK NTX POINT OF CARE (POC) CONTROL SET
Chemistry
35d