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FDA 510(k)

LINDE OXYGEN THERAPY FLOWMETERS, L33-L34

K-Number: K791069 · 1979-06-27

ApplicantUnion Carbide Corp.
Decision Date1979-06-27
Product CodeCAX
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LINDE OXYGEN THERAPY FLOWMETERS, L33-L34 is the device name listed in this FDA 510(k) record. The listed applicant is Union Carbide Corp.. It received FDA 510(k) clearance on 1979-06-27 under 510(k) number K791069. 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 LINDE OXYGEN THERAPY FLOWMETERS, L33-L34?

LINDE OXYGEN THERAPY FLOWMETERS, L33-L34 is a medical device that received FDA 510(k) clearance on 1979-06-27. The listed applicant is Union Carbide Corp.. The 510(k) number is K791069.

When did LINDE OXYGEN THERAPY FLOWMETERS, L33-L34 receive FDA 510(k) clearance?

LINDE OXYGEN THERAPY FLOWMETERS, L33-L34 received FDA 510(k) clearance on 1979-06-27, under 510(k) number K791069.

Who is the listed applicant for LINDE OXYGEN THERAPY FLOWMETERS, L33-L34?

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

What is the FDA product code for LINDE OXYGEN THERAPY FLOWMETERS, L33-L34?

The FDA product code for LINDE OXYGEN THERAPY FLOWMETERS, L33-L34 is CAX.

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Other records listing Union Carbide Corp. as applicant

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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

View on FDA Database →

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

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