Product code KGZ— General, Plastic Surgery
3-WAY STOPCOCK WITH LUER-LOCK FITTING
- Classification name
- Accessories, Catheter
- Device class
- Class 1
- Regulation
- 21 CFR 878.4200
- Advisory panel
- General, Plastic Surgery
- Total cleared
- 29
- First cleared
- Most recent
Market context for product code KGZ
FDA has cleared devices under product code KGZ between 1976 and 2002, filed by 23 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Clearances per year
last 15 years- 2002
- 1998
- 1996
- 1994
- 1989
- 1987
- 1986
- 1984
- 1982
- 1981
- 1980
- 1979
- 1978
- 1977
- 1976
Top applicants under product code KGZ
Recent clearances under product code KGZ
- K022306 — AART SILICONE TUBING
- K974295 — BYRON MEDICAL ASPIRATION AND INFILTRATION/IRRIGATION TUBING
- K973183 — WOUND DRAINAGE HOLDER
- K955433 — DURALASTIC SILICONE TUBING
- K942315 — NAVARRE PERCUTANEOUS ACCESS SET
- K896087 — PALESTRANT IRRIGATION AND DRAINAGE SET
- K895041 — OPTICAL CATHETER(TM) INTRODUCER SETS
- K893406 — DESERET PRN ADAPTER
- K873009 — CONCEPT SWITCHING STICK
- K870014 — HCI GENERAL PURPOSE CATHETER STYLET
- K864115 — TUBEGRIPPER, DRAINAGE CATHETER & ACCESSORY FOR SU
- K855078 — ANGIO MED DISPOSABLE PRESSURE CONNECTORS
- K842666 — NU-THOR THORACOSTOMY KIT
- K821525 — DESERET UNIVERSAL LUER LOCK
- K821245 — DESERET OFFSET PRN ADAPTER
- K810530 — PERI-PATCH GLUE MOLD
- K810531 — PERI-PATCH PERITONEAL CATHETER EXTENSION
- K802286 — ARGLE LATEX PENROSE TUBING
- K802367 — ARROW CATHETER CLAMP
- K791803 — CONPHAR CATHETER PLUG
- K791806 — CONPHAR ADAPT-CONNECTS STERILE, NONSTE.
- K790597 — SENSOMAT SIDEARM ADAPTER
- K781846 — ADAPTER, CATHETER SHEATH
- K781854 — PAD, B-D I.V. CATH.
- K780259 — CATHETERIZATION TRAY & KIT
- K770154 — 3-WAY STOPCOCK WITH LUER-LOCK FITTING
- K760383 — STOPCOCKS
- K760384 — STOPPERS
- K760385 — EXTENSION SETS
Data sourced from openFDA. This site is unofficial and independent of the FDA.