FDA 510(k)

MO8 OXYGEN FLOWMETER

K-Number: K802311 · 1980-10-23

Decision Date1980-10-23

Product CodeCAX

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

MO8 OXYGEN FLOWMETER is the device name listed in this FDA 510(k) record. The listed applicant is Timeter Instrument Corp.. It received FDA 510(k) clearance on 1980-10-23 under 510(k) number K802311. The device is classified under product code CAX. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MO8 OXYGEN FLOWMETER?

MO8 OXYGEN FLOWMETER is a medical device that received FDA 510(k) clearance on 1980-10-23. The listed applicant is Timeter Instrument Corp.. The 510(k) number is K802311.

When did MO8 OXYGEN FLOWMETER receive FDA 510(k) clearance?

MO8 OXYGEN FLOWMETER received FDA 510(k) clearance on 1980-10-23, under 510(k) number K802311.

Who is the listed applicant for MO8 OXYGEN FLOWMETER?

The FDA 510(k) record lists Timeter Instrument Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MO8 OXYGEN FLOWMETER?

The FDA product code for MO8 OXYGEN FLOWMETER is CAX.

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Other records listing Timeter Instrument Corp. as applicant

K875075RT-200 COMPUTER INTERFACE K875074VACUMATE INTERMITTENT/CONTINUOUS CONTROLLER,VM2000 K871603CRITERION II & IIA OXYGEN CONCENTRATORS K864836L.A.P. SPIROMETER K834274CRITERION I K823775BORDON GAGE REGULATOR #BG

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Related Devices (Code: CAX)

K923781MXR-2000 FLOWMETERPorter Instrument Co., Inc.K910316OHMEDA - LOW FLOW FLOWMETEROhmeda Medical K884973FR6000 FLOWMETERKey Instruments K872718SERIES D FLOWMETERPuritan Bennett Corp.K871452CLASSIC (TM) 200 OXYGEN FLOWMETERThe Timeter Group K862797AIRCO 2000 SERIES FLOWMETERSAirco, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.