MED-WEST DUAL LUMEN INTERNAL JUGULAR CATHETER— 510(k) K905080

Name: FDA 510(k) clearance K905080
Creator: U.S. Food and Drug Administration
Published: 1991-01-31

Substantially Equivalent

Kendall Healthcare Products Co. Div.Of Tyco Health

FDA 510(k) clearance K905080 for MED-WEST DUAL LUMEN INTERNAL JUGULAR CATHETER, Substantially Equivalent on 1991-01-31. Applicant: Kendall Healthcare Products Co. Div.Of Tyco Health. Device class: 2.

Clearance details

Applicant: Kendall Healthcare Products Co. Div.Of Tyco Health
Product code: Code LFJ
Device class: Class 2
Regulation: 21 CFR 876.5540
Advisory panel: Gastroenterology, Urology
Date received: 1990-11-13
Decision date: 1991-01-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mansfield, MA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LFJ

view all

K920780 — MEDSURG INSERTION TRAY1994-08-19
K925819 — AKCESS0CATH KIT1994-08-02
K925818 — AKCESS-CATH1994-04-05
K913468 — ULDALL DOUBLE LUMEN HEMODIALYSIS CATHETER SET/TRAY1994-03-24
K920634 — SPLITTABLE SHEATH INTRODUCER SET1994-01-14

More clearances from Kendall Healthcare Products Co. Div.Of Tyco Health

view all

K973763 — KENDALL CURITY IODOFORM PACKING STRIP1997-12-31
K973511 — KENDALL CURITY PETROLATUM GAUZE1997-12-16
K973507 — KENDALL XEROFORM PETROLATUM DRESSING (6311,6312,6313,6314,6315,6316,6317)1997-12-15
K973619 — KENDALL CURITY NON-ADHERING DRESSING1997-12-10
K973509 — KENDALL CURASORB ZN + MG ALGINATE WOUND DRESSING1997-12-04

Data sourced from openFDA. This site is unofficial and independent of the FDA.