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North American Sterilization & Packaging Co.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
16
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K964231NASP HYDROCOLLOID DRESSING (REGULAR OR THIN)March 10, 1997
K963753NASP TRANSPARENT DRESSINGNovember 29, 1996
K962352HYDROGEL SKIN DRESSINGAugust 2, 1996
K925593NORTEC STERILE WATER FOR DEVICE IRRIGATIONDecember 3, 1993
K925588NORTEC STER SALINE-O.9% SODIUM CHLOR FOR DEV IRRIDecember 3, 1993
K925161NORTEC STERILE WATER FOR CATHETER BALLOON INFLATIOJuly 21, 1993
K911865NORTEC CONNECTING TUBE SETNovember 1, 1991
K911784NORTEC ROBERTAZZI NASOPHARYNGEAL AIRWAYSeptember 23, 1991
K910691NORTEC URETERAL STENTAugust 15, 1991
K903162FLEXIBLE ENDOSCOPIC ELECTRODESDecember 18, 1990
K903156CONTROL-TIP CYSTOSCOPIC ELECTRODESDecember 18, 1990
K902763STERILE INSTRUMENT DRAPESeptember 20, 1990
K896821OLYMPUS URETERO. & CIRCON ACMI URETERO. GUIDEFebruary 9, 1990
K900401NAS&P GRASPING FORCEPS & ASSOC. DEVICESFebruary 9, 1990
K894939PERCUTANEOUS ENDOSCOPIC GASTROSTOMY TRAYDecember 8, 1989
K8949863-RING HANDLE, GRASP FORCEPS, LOOP RETRIE., BASKETDecember 1, 1989