CONNECTING TUBING— 510(k) K831082

Name: FDA 510(k) clearance K831082
Creator: U.S. Food and Drug Administration
Published: 1983-05-09

Substantially Equivalent

The Kendall Company Div. of Tyco Healthcare Group

FDA 510(k) clearance K831082 for CONNECTING TUBING, Substantially Equivalent on 1983-05-09. Applicant: The Kendall Company Div. of Tyco Healthcare Group. Device class: 1.

Clearance details

Applicant: The Kendall Company Div. of Tyco Healthcare Group
Product code: Code BYX
Device class: Class 1
Regulation: 21 CFR 868.5860
Advisory panel: Anesthesiology
Date received: 1983-04-04
Decision date: 1983-05-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code BYX

view all

K011134 — OXYGEN SUPPLY TUBING, MODEL 11152001-06-13
K955656 — NORTH STATE PLASTICS AEROSOL TEE1996-03-06
K943110 — GAS SAMPLING INTERFACES1994-08-19
K935835 — BUSSE PLASTIC TUBING CONNECTORS AND ACCESSORIES1994-01-12
K931033 — MF CHEMETRON STYLE MEDICAL GAS WALL OUTLETS1993-06-01

More clearances from The Kendall Company Div. of Tyco Healthcare Group

view all

K024010 — DOVER SILVER HYDROGEL COATED SILICONE FOLEY CATHETER2003-06-11
K831081 — EZEE FILTER/SEPARATOR1983-05-16
K831079 — LIQUIPETTE1983-04-28

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