OXYGEN REGULATOR
K-Number: K950777 · 1995-04-14
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Device Summary
Frequently Asked Questions
What is the OXYGEN REGULATOR?
OXYGEN REGULATOR is a medical device that received FDA 510(k) clearance on 1995-04-14. The listed applicant is Mada Medical Products, Inc.. The 510(k) number is K950777.
When did OXYGEN REGULATOR receive FDA 510(k) clearance?
OXYGEN REGULATOR received FDA 510(k) clearance on 1995-04-14, under 510(k) number K950777.
Who is the listed applicant for OXYGEN REGULATOR?
The FDA 510(k) record lists Mada Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OXYGEN REGULATOR?
The FDA product code for OXYGEN REGULATOR is CAN.
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 Mada Medical Products, 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: CAN)
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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