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FDA 510(k)

MARK III OXYGEN WALKER SYS. RESERVOIR

K-Number: K832143 · 1983-08-26

ApplicantLinde Div. Union Carbide Corp.
Decision Date1983-08-26
Product CodeBYJ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MARK III OXYGEN WALKER SYS. RESERVOIR is the device name listed in this FDA 510(k) record. The listed applicant is Linde Div. Union Carbide Corp.. It received FDA 510(k) clearance on 1983-08-26 under 510(k) number K832143. The device is classified under product code BYJ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MARK III OXYGEN WALKER SYS. RESERVOIR?

MARK III OXYGEN WALKER SYS. RESERVOIR is a medical device that received FDA 510(k) clearance on 1983-08-26. The listed applicant is Linde Div. Union Carbide Corp.. The 510(k) number is K832143.

When did MARK III OXYGEN WALKER SYS. RESERVOIR receive FDA 510(k) clearance?

MARK III OXYGEN WALKER SYS. RESERVOIR received FDA 510(k) clearance on 1983-08-26, under 510(k) number K832143.

Who is the listed applicant for MARK III OXYGEN WALKER SYS. RESERVOIR?

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

What is the FDA product code for MARK III OXYGEN WALKER SYS. RESERVOIR?

The FDA product code for MARK III OXYGEN WALKER SYS. RESERVOIR is BYJ.

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Other records listing Linde Div. Union Carbide Corp. as applicant

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.

K882208MEDIBLEND (TM) MEDICAL LASER GAS MIXTURESK882209MEDIBLEND (TM) CLINICAL BLOOD GAS MIXTURESK882210MEDIBLEND (TM) LUNG DIFFUSION GAS MIXTURESK823582OXYGEN CONCENTRATOR UCC-100K821841MEDIGAS SUCTION/DRAINAGE EQUIPMENT

Related Devices (Code: BYJ)

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.

K130068DISMOUNTED MEDICAL & SUPPLEMENTAL OXYGEN SYSTEM (DMOS)Essex Industries, Inc. D/B/A Essex Cryogenics of MK113767MOUNTED MEDICAL OXYGEN SYSTEMEssex Industries, Inc.K103324PRECISION LIQUID OXYGEN SYSTEMPrecision Medical, Inc.K101272MASS OXYGEN DISTRIBUTION SYSTEM (MODS) MODEL 10C-0061-3Essex Industries, Inc.K081779GOLOX-93Respironics, Inc.K080023MODIFICATION TO: SPIRITCaire, 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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