Teknar, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
18
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K903666OPHTHASONIC A/P IIINovember 19, 1990
K896038B-SCAN 10 MHZ PROBEApril 23, 1990
K896150IMAGE 2000 SYSTEM, IMAGING, ULTRA-SONICJanuary 18, 1990
K891777PRO-CUT BIOPSY NEEDLEMay 4, 1989
K883965PROBE, IMAGING, ULTRASONIC, MECHANICAL SECTOROctober 5, 1988
K881850TEKNAR PERCU-SCANAugust 29, 1988
K881605BIOPSY GUIDEJune 21, 1988
K880659TEKNAR PROSCAN ACCESSORY PROBEApril 14, 1988
K871536OPHTHASONIC A-SCAN/ B-SCANAugust 26, 1987
K864807TEKNAR PROSCAN(TM)July 10, 1987
K860757OPHTHASONIC A-SCANDecember 18, 1986
K850116BETASONIC IIIMarch 29, 1985
K834539AXIPAC IISeptember 11, 1984
K830474IV STANDApril 5, 1983
K823011VC IIINovember 8, 1982
K822900FISCH DRILL PUMPNovember 8, 1982
K810697AXISONIC IIJuly 13, 1981
K801314VOCON MODEL VC526September 9, 1980