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Snowden-Pencer

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K960400DIAMOND-TOUCH AND MICRO DIAMOND-TOUCH INSTRUMENTS/DIAMOND-LINE INSTRUMENTS/DIAMOND-PORT(ACCESS PARTSMarch 12, 1996
K930666REUSABLE LAPAROSCOPIC INSTRUMENTS W/ ELECTROCAUTERYMay 19, 1994
K930667REUSABLE LAPAROSCOPIC INSTRUMENTSMay 16, 1994
K924148DIAMOND-SHARP(R) TROCARSFebruary 28, 1994
K924149ENDO I/A PROBEJanuary 26, 1993
K920985SNOWDEN-PENCER IRRIGATION PUMPJune 9, 1992
K920986SNOWDEN-PENCER HIGH FLOW INSUFFLATOR, SP/88-9700June 4, 1992
K913979ENDO I/A Y SETNovember 27, 1991
K913835SNOWDEN-PENCER INSUFFLATOR TUBING SETNovember 7, 1991
K861372ELECTROSURGICAL CUTTING AND COAGULATION ACCESSORYJune 19, 1986