OXYGEN BARB M-552
K-Number: K790934 · 1979-05-21
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Device Summary
Frequently Asked Questions
What is the OXYGEN BARB M-552?
OXYGEN BARB M-552 is a medical device that received FDA 510(k) clearance on 1979-05-21. The listed applicant is Mem Medical, Inc.. The 510(k) number is K790934.
When did OXYGEN BARB M-552 receive FDA 510(k) clearance?
OXYGEN BARB M-552 received FDA 510(k) clearance on 1979-05-21, under 510(k) number K790934.
Who is the listed applicant for OXYGEN BARB M-552?
The FDA 510(k) record lists Mem Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OXYGEN BARB M-552?
The FDA product code for OXYGEN BARB M-552 is BYG.
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 Mem Medical, Inc. 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: BYG)
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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