LINDE OXYGEN CONCENTRATOR LOC-II
K-Number: K791437 · 1979-09-19
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Device Summary
Frequently Asked Questions
What is the LINDE OXYGEN CONCENTRATOR LOC-II?
LINDE OXYGEN CONCENTRATOR LOC-II is a medical device that received FDA 510(k) clearance on 1979-09-19. The listed applicant is Union Carbide Corp.. The 510(k) number is K791437.
When did LINDE OXYGEN CONCENTRATOR LOC-II receive FDA 510(k) clearance?
LINDE OXYGEN CONCENTRATOR LOC-II received FDA 510(k) clearance on 1979-09-19, under 510(k) number K791437.
Who is the listed applicant for LINDE OXYGEN CONCENTRATOR LOC-II?
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 LOC-II?
The FDA product code for LINDE OXYGEN CONCENTRATOR LOC-II is CAW.
Related Clinical Trials
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.
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.
Related Devices (Code: CAW)
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.
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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