Kli

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
18
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K800822CO2 CYSTOSCOPY/URETHROSCOPY CONSOLEJune 17, 1980
K800913GYNECOLOGICAL CYSTO/URETHROSCOPEMay 14, 1980
K781913INSUFFALATOR LAPARAOSCOPICDecember 4, 1978
K781109FORCEPS, ELECTROSURGICALSeptember 14, 1978
K781089ONE INCISION BI-POLAR ELECTRO. FORCEPSJuly 17, 1978
K780955SCISSORS, HOOK, ELECTROSURGICALJune 22, 1978
K780954SCISSORS, HOOK, ELECTROSURGICALJune 22, 1978
K772297INSUFFLATOR, MODEL G100 & 200January 5, 1978
K772242LAPAROSCOPY CONSOLE MODEL VIIIDecember 20, 1977
K772220PROBE, COAGULATION ACCESSORYDecember 13, 1977
K772185LAPAROSCOPE W/REMOVABLE OPTICSNovember 30, 1977
K771962CAMERA ADAPTER FOR ENDOSCOPESNovember 21, 1977
K7719598MM SELF-SEALING TROCAR & CANNULAOctober 25, 1977
K77195812MM SELF-SEALING TROCAR & CANNULAOctober 25, 1977
K771960TUBAL OCCLUSION INSERTER/LAPAROSCOPEOctober 25, 1977
K771961DUAL INCISION TUBAL OCCLUS. BAND APPLI.October 25, 1977
K7719648MM TROCAR & CANNUAL W/STOPCOCKOctober 25, 1977
K771963SINGLE INCISION TUBAL OCCLU. BAND APPL.October 25, 1977