Stephen Chakoff, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Stephen Chakoff, Inc. - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
Stephen Chakoff, Inc. has 16 FDA 510(k) cleared general & plastic surgery devices. Based in Miami, US.
Historical record: 16 cleared submissions from 1993 to 1995.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Stephen Chakoff, Inc.
16 devices
Cleared
Nov 16, 1995
HYSTERSCOPE
Obstetrics & Gynecology
661d
Cleared
May 24, 1995
SINUSCOPE
Ear, Nose, Throat
485d
Cleared
May 15, 1995
CHAKOFF ENDOSCOPY (CAMERA TELEVISION ENDOSCOPIC WITHOUT AUDIO
General & Plastic Surgery
87d
Cleared
Mar 22, 1995
CHAKOFF ENDOSCOPY, RIGID ENDOSCOPE
General & Plastic Surgery
13d
Cleared
Mar 06, 1995
CHAKOFF ENDOSCOPY (RIDGID ENDOSCOPE)
General & Plastic Surgery
17d
Cleared
Mar 06, 1995
CHAKOFF ENDOSCOPY (ENDOSCOPE AND/OR ACCESSORIES)
General & Plastic Surgery
17d
Cleared
Mar 06, 1995
CHAKOFF ENDOSCOPY (SET LAPAROSCOPY)
General & Plastic Surgery
17d
Cleared
Mar 06, 1995
CHAKOFF ENDOSCOPY (LIGHT SOURCE ENDOSCOPIC XENON ARC.)
General & Plastic Surgery
17d
Cleared
Mar 06, 1995
CHAKOFF ENDOSCOPY (FIBER OPTIC LIGHT SOURCE ROUTINE)
General & Plastic Surgery
17d
Cleared
Dec 23, 1994
CHAKOFF ENDOSCOPY
Gastroenterology & Urology
49d
Cleared
Dec 08, 1994
CHAKOFF ENDOSCOPY
Gastroenterology & Urology
34d
Cleared
Jun 21, 1994
CHAKOFF ENDOSCOPY LAPAROSCOPIC INSTRUMENTATION
General & Plastic Surgery
385d
Cleared
Feb 04, 1994
CHAKOFF ENDOSCOPY
General & Plastic Surgery
248d
Cleared
Nov 16, 1993
FIBER OPTIC LIGHT CABLE
General & Plastic Surgery
168d
Cleared
Nov 16, 1993
XENON LIGHT SOURCE ILLUMINATOR
General & Plastic Surgery
168d
Cleared
Oct 15, 1993
ENDOSCOPIC VIDEO CAMERA
General & Plastic Surgery
136d