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FDA 510(k)

LINDE OXYGEN CONCENTRATOR MODEL LOC-HCA

K-Number: K781454 · 1978-09-20

ApplicantUnion Carbide Corp.
Decision Date1978-09-20
Product CodeCHW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LINDE OXYGEN CONCENTRATOR MODEL LOC-HCA 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 1978-09-20 under 510(k) number K781454. The device is classified under product code CHW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LINDE OXYGEN CONCENTRATOR MODEL LOC-HCA?

LINDE OXYGEN CONCENTRATOR MODEL LOC-HCA is a medical device that received FDA 510(k) clearance on 1978-09-20. The listed applicant is Union Carbide Corp.. The 510(k) number is K781454.

When did LINDE OXYGEN CONCENTRATOR MODEL LOC-HCA receive FDA 510(k) clearance?

LINDE OXYGEN CONCENTRATOR MODEL LOC-HCA received FDA 510(k) clearance on 1978-09-20, under 510(k) number K781454.

Who is the listed applicant for LINDE OXYGEN CONCENTRATOR MODEL LOC-HCA?

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 CONCENTRATOR MODEL LOC-HCA?

The FDA product code for LINDE OXYGEN CONCENTRATOR MODEL LOC-HCA is CHW.

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Other records listing 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.

K830337MARK III OXYGEN WALKER SYS-LOW PRESSK820836MARK III OXYGEN WALKER SYSTEMK820535LASER GAS MIXTURESK812536LINDE MARK IIK810732LINDE MARK II OXYGEN RESERV. TYPE OR-4K810596CENTRIFI CHEM SYSTEM 400 ANALYZER

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Related Devices (Code: CHW)

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.

K192730CALCIUM-CRESOLPHTHALEIN, GLUCOSE, UREA/BUN-UVBiosystems S.A.K113521CALCIUM GEN. 2Roche Diagnostics

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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