MOXUS OR OCM-1 OXYGEN UPTAKE SYSTEM— 510(k) K874663

Name: FDA 510(k) clearance K874663
Creator: U.S. Food and Drug Administration
Published: 1988-05-31

Substantially Equivalent

Ametek/Thermox Instruments Division

FDA 510(k) clearance K874663 for MOXUS OR OCM-1 OXYGEN UPTAKE SYSTEM, Substantially Equivalent on 1988-05-31. Applicant: Ametek/Thermox Instruments Division. Device class: 2.

Clearance details

Applicant: Ametek/Thermox Instruments Division
Product code: Code BZL
Device class: Class 2
Regulation: 21 CFR 868.1730
Advisory panel: Anesthesiology
Date received: 1987-11-13
Decision date: 1988-05-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pittsburgh, PA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code BZL

view all

K200076 — Breezing Med2020-09-25
K190561 — NICU V'022020-09-04
K110810 — ANASCIENT BREATH MONITOR2011-06-21
K093080 — METAPHOR METABOLIC MONITOR2010-01-22
K071533 — FITMATE SERIES2007-09-28

More clearances from Ametek/Thermox Instruments Division

view all

K875183 — LC OXYGEN ANALYZER1988-03-29

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