Scholten Surgical Instruments, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
8
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K072051NOVATOME, MODEL: SU101-50October 3, 2007
K900405SCHOLTEN FRAMEMarch 1, 1990
K852331SYS, ANGIOGRAPHIC, SINGLE-OR BI-PLANE RADIOGRAPHICAugust 1, 1986
K852119TEMPORARY PACEMAKER GROUND WIRESeptember 15, 1985
K852332TABLE ACCESSORIES, OPERATING ROOMJuly 2, 1985
K852120FORCEPS, BIOPSY(NON RIGID)July 2, 1985
K852330RETRACTOR, SURGICALJune 27, 1985
K852329STAND, OPERATING ROOMJune 14, 1985