OXYMIZER FLOW RESTRICTOR
K-Number: K841901 · 1984-07-23
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Device Summary
Frequently Asked Questions
What is the OXYMIZER FLOW RESTRICTOR?
OXYMIZER FLOW RESTRICTOR is a medical device that received FDA 510(k) clearance on 1984-07-23. The listed applicant is Chad Therapeutics, Inc.. The 510(k) number is K841901.
When did OXYMIZER FLOW RESTRICTOR receive FDA 510(k) clearance?
OXYMIZER FLOW RESTRICTOR received FDA 510(k) clearance on 1984-07-23, under 510(k) number K841901.
Who is the listed applicant for OXYMIZER FLOW RESTRICTOR?
The FDA 510(k) record lists Chad Therapeutics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OXYMIZER FLOW RESTRICTOR?
The FDA product code for OXYMIZER FLOW RESTRICTOR is BYX.
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 Chad Therapeutics, 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: BYX)
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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