OXYGEN HOODS
K-Number: K791861 · 1979-10-04
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Device Summary
Frequently Asked Questions
What is the OXYGEN HOODS?
OXYGEN HOODS is a medical device that received FDA 510(k) clearance on 1979-10-04. The listed applicant is Ann Arbor Plastics, Inc.. The 510(k) number is K791861.
When did OXYGEN HOODS receive FDA 510(k) clearance?
OXYGEN HOODS received FDA 510(k) clearance on 1979-10-04, under 510(k) number K791861.
Who is the listed applicant for OXYGEN HOODS?
The FDA 510(k) record lists Ann Arbor Plastics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OXYGEN HOODS?
The FDA product code for OXYGEN HOODS is FOG.
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 Ann Arbor Plastics, 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: FOG)
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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