OXYGENERATOR NO. M-049
K-Number: K790927 · 1979-05-21
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Device Summary
Frequently Asked Questions
What is the OXYGENERATOR NO. M-049?
OXYGENERATOR NO. M-049 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 K790927.
When did OXYGENERATOR NO. M-049 receive FDA 510(k) clearance?
OXYGENERATOR NO. M-049 received FDA 510(k) clearance on 1979-05-21, under 510(k) number K790927.
Who is the listed applicant for OXYGENERATOR NO. M-049?
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 OXYGENERATOR NO. M-049?
The FDA product code for OXYGENERATOR NO. M-049 is BTR.
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: BTR)
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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