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Stephen Chakoff, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K940316HYSTERSCOPENovember 16, 1995
K940317SINUSCOPEMay 24, 1995
K950753CHAKOFF ENDOSCOPY (CAMERA TELEVISION ENDOSCOPIC WITHOUT AUDIOMay 15, 1995
K951082CHAKOFF ENDOSCOPY, RIGID ENDOSCOPEMarch 22, 1995
K950744CHAKOFF ENDOSCOPY (RIDGID ENDOSCOPE)March 6, 1995
K950748CHAKOFF ENDOSCOPY (FIBER OPTIC LIGHT SOURCE ROUTINE)March 6, 1995
K950747CHAKOFF ENDOSCOPY (LIGHT SOURCE ENDOSCOPIC XENON ARC.)March 6, 1995
K950745CHAKOFF ENDOSCOPY (ENDOSCOPE AND/OR ACCESSORIES)March 6, 1995
K950746CHAKOFF ENDOSCOPY (SET LAPAROSCOPY)March 6, 1995
K945421CHAKOFF ENDOSCOPYDecember 23, 1994
K945420CHAKOFF ENDOSCOPYDecember 8, 1994
K932632CHAKOFF ENDOSCOPY LAPAROSCOPIC INSTRUMENTATIONJune 21, 1994
K932627CHAKOFF ENDOSCOPYFebruary 4, 1994
K932631XENON LIGHT SOURCE ILLUMINATORNovember 16, 1993
K932629FIBER OPTIC LIGHT CABLENovember 16, 1993
K932628ENDOSCOPIC VIDEO CAMERAOctober 15, 1993