PORTAGAS AERATOR
K-Number: K761341 · 1977-02-28
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Device Summary
Frequently Asked Questions
What is the PORTAGAS AERATOR?
PORTAGAS AERATOR is a medical device that received FDA 510(k) clearance on 1977-02-28. The listed applicant is Amsco Co.. The 510(k) number is K761341.
When did PORTAGAS AERATOR receive FDA 510(k) clearance?
PORTAGAS AERATOR received FDA 510(k) clearance on 1977-02-28, under 510(k) number K761341.
Who is the listed applicant for PORTAGAS AERATOR?
The FDA 510(k) record lists Amsco Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PORTAGAS AERATOR?
The FDA product code for PORTAGAS AERATOR is FLI.
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 Amsco Co. 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: FLI)
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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