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FDA 510(k)

OXYGEN DELIVERY MEASURING DEVICE

K-Number: K851288 · 1985-09-03

ApplicantBar-Dix, Inc.
Decision Date1985-09-03
Product CodeCAX
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OXYGEN DELIVERY MEASURING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Bar-Dix, Inc.. It received FDA 510(k) clearance on 1985-09-03 under 510(k) number K851288. 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 OXYGEN DELIVERY MEASURING DEVICE?

OXYGEN DELIVERY MEASURING DEVICE is a medical device that received FDA 510(k) clearance on 1985-09-03. The listed applicant is Bar-Dix, Inc.. The 510(k) number is K851288.

When did OXYGEN DELIVERY MEASURING DEVICE receive FDA 510(k) clearance?

OXYGEN DELIVERY MEASURING DEVICE received FDA 510(k) clearance on 1985-09-03, under 510(k) number K851288.

Who is the listed applicant for OXYGEN DELIVERY MEASURING DEVICE?

The FDA 510(k) record lists Bar-Dix, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OXYGEN DELIVERY MEASURING DEVICE?

The FDA product code for OXYGEN DELIVERY MEASURING DEVICE is CAX.

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Related Devices (Code: CAX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K923781MXR-2000 FLOWMETERPorter Instrument Co., Inc.K910316OHMEDA - LOW FLOW FLOWMETEROhmeda MedicalK884973FR6000 FLOWMETERKey InstrumentsK872718SERIES D FLOWMETERPuritan Bennett Corp.K871452CLASSIC (TM) 200 OXYGEN FLOWMETERThe Timeter GroupK862797AIRCO 2000 SERIES FLOWMETERSAirco, Inc.

Official Source

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

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