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Optus, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
10
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K945264OPTUS OTOSCOPESFebruary 2, 1996
K953913OPTUS ARTHROSCOPE & MINI-ARTHROSCOPE ACCESSORIESJanuary 22, 1996
K945268OPTUS BRONCHOSCOPESDecember 21, 1995
K945265OPTUS HYSTEROSCOPES AND CONTACT HYSTEROSCOPESSeptember 12, 1995
K945262OPTUS CYSTOSCOPES AND PEDIATRIC CYSTOSCOPESMay 26, 1995
K945267OPTUS ARTHROSCOPES AND MINI-ARTHROSCOPESMay 23, 1995
K945266OPTUS LAPAROSCOPES AND OPERATING LAPAROSCOPESFebruary 23, 1995
K944656OPTUS SINUSCOPES AND ACCESSORIESJanuary 26, 1995
K945263OPTUS THORACOSCOPESDecember 13, 1994
K945269OPTUS LARYNGOSCOPESNovember 7, 1994