MEDIPART XENON BREATHING KIT MP-02XM-I— 510(k) K850367

Name: FDA 510(k) clearance K850367
Creator: U.S. Food and Drug Administration
Published: 1985-04-30

Substantially Equivalent

Medipart Jerry Alexander

FDA 510(k) clearance K850367 for MEDIPART XENON BREATHING KIT MP-02XM-I, Substantially Equivalent on 1985-04-30. Applicant: Medipart Jerry Alexander. Device class: 2.

Clearance details

Applicant: Medipart Jerry Alexander
Product code: Code IYT
Device class: Class 2
Regulation: 21 CFR 892.1390
Advisory panel: Radiology
Date received: 1985-01-30
Decision date: 1985-04-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cary, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IYT

view all

K253942 — Pulmonex II Xenon System (132-503)2026-07-07
K200916 — Patient Administration Set2020-09-01
K953513 — XENON CIRCUIT1995-11-03
K952223 — XENON GAS BREATHING CIRCUIT1995-08-11
K914747 — XENON CIRCUIT1992-02-27

More clearances from Medipart Jerry Alexander

view all

K896885 — DISPOSABLE RESPIRTORY KIT (MP-200)1990-02-26
K896125 — MEDIPART DISPOSABLE XENON-133 REBREATHING MP-0133M1990-02-01
K896124 — MEDIPART DISPOSABLE XENON-133 REBREATHING MP-01331990-01-22
K896475 — DISP. RADIOAEROSOL KIT (MP-400) TO FIT LEAD SHIELD1990-01-22
K896476 — DISP. RADIOAEROSOL KIT (MP-400-M) TO FIT SHIELD1990-01-22

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