Dexide, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
38
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K991814MULTACHOICE INSTRUMENTSJune 23, 1999
K990379MODIFICATION TO MULTAPORT CANNULA, REDUCER AND ACCESSORIESMarch 4, 1999
K981940MULTAPUMP DISPOSABLE PUMP HEAD AND ACCESSORIESSeptember 25, 1998
K981941MULTAPORT CANNULA REDUCER AND ACCESSORIESJuly 29, 1998
K953611DEXIDE ENDO-LUBE KITSeptember 15, 1995
K944509DEXIDE INSUFFLATION TUBING WITH FILTERFebruary 7, 1995
K924117DEXIDE LAPAROSCOPIC KITSMarch 23, 1993
K923845DEXIDE LAPAROSCOPIC ACCESSORIESNovember 25, 1992
K921709ENDOBAG, MODIFICATIONJuly 14, 1992
K913762MONOSCOPY(TM) BRAND, ENDOBAGOctober 28, 1991
K912637LAPAROSCOPIC ELECTROSURGICAL CANNULA W/RETRACTABLEOctober 4, 1991
K912862MONOSCOPY(TM) BRANK, HOOK DISSECTORAugust 12, 1991
K912750MONOSCOPY(TM) BRAND, DUAL SUCTION/IRRIGATION CONTRAugust 2, 1991
K913104MONOSCOPY(TM) BRAND, ELECTROSURGICAL RAKEJuly 31, 1991
K912980MONOSCOPY BRAND 5MM LOCK TROCAR SLEEVE, MODIFIEDJuly 26, 1991
K912343DISTENDABLE PALPATION PROBEJune 18, 1991
K905549THE DARTFebruary 19, 1991
K902563MONOSCOPY(TM) BRAND, TROCAR REDUCER SETSeptember 4, 1990
K896205MONOSCOPY BRAND, 5 MM LOCKING TROCAR SLEEVEMarch 22, 1990
K893527LAPAROSCOPIC SUCTION PROBEJuly 14, 1989