Metrika, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
11
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K051321INVIEWJune 13, 2005
K033847A1CNOW FOR HOME AND PROFESSIONAL USEDecember 23, 2003
K022661A1CNOW FOR HOME USEDecember 13, 2002
K020235A1CNOW FOR PROFESSIONAL USEFebruary 15, 2002
K020234A1CNOW FOR RX HOME USEFebruary 15, 2002
K000885DRX HBA1C - FOR PRESCRIPTION HOME USESeptember 26, 2000
K000887DRX HBA1CJuly 26, 2000
K992997OSTEOMARK NTX POCNovember 9, 1999
K991532DRX QT. HCGSeptember 17, 1999
K984530DRX NTX OR, OSTEOMARK NTX DIRECT RESPONSEAugust 10, 1999
K991917OSTEOMARK NTX POINT OF CARE (POC) CONTROL SETJuly 12, 1999