Stephen Chakoff, Inc.
Stephen Chakoff, Inc. holds FDA 510(k) medical device clearances, first cleared 1993, most recent 1995.
Top product codes for Stephen Chakoff, Inc.
Recent clearances by Stephen Chakoff, Inc.
- K940316 — HYSTERSCOPE
- K940317 — SINUSCOPE
- K950753 — CHAKOFF ENDOSCOPY (CAMERA TELEVISION ENDOSCOPIC WITHOUT AUDIO
- K951082 — CHAKOFF ENDOSCOPY, RIGID ENDOSCOPE
- K950744 — CHAKOFF ENDOSCOPY (RIDGID ENDOSCOPE)
- K950745 — CHAKOFF ENDOSCOPY (ENDOSCOPE AND/OR ACCESSORIES)
- K950746 — CHAKOFF ENDOSCOPY (SET LAPAROSCOPY)
- K950747 — CHAKOFF ENDOSCOPY (LIGHT SOURCE ENDOSCOPIC XENON ARC.)
- K950748 — CHAKOFF ENDOSCOPY (FIBER OPTIC LIGHT SOURCE ROUTINE)
- K945421 — CHAKOFF ENDOSCOPY
- K945420 — CHAKOFF ENDOSCOPY
- K932632 — CHAKOFF ENDOSCOPY LAPAROSCOPIC INSTRUMENTATION
- K932627 — CHAKOFF ENDOSCOPY
- K932629 — FIBER OPTIC LIGHT CABLE
- K932631 — XENON LIGHT SOURCE ILLUMINATOR
- K932628 — ENDOSCOPIC VIDEO CAMERA
Data sourced from openFDA. This site is unofficial and independent of the FDA.