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Endooptiks, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K083788ENDO OPTIKS UROLOGICAL CATHETER FOR ENDOSCOPY, MODEL SESSRMarch 3, 2009
K042918MICROPROBE LASER AND ENDOSCOPY SYSTEM, MODEL E2November 22, 2004
K003151MICROPOBE SERIES OF LASERS AND ACCESSORIESJanuary 8, 2001
K945081TRANSTYMPANIC ENDOSCOPEMarch 6, 1995
K922917ENDOPROBESSeptember 28, 1992