OXYLOG 2
K-Number: K954731 · 1997-01-06
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Device Summary
Frequently Asked Questions
What is the OXYLOG 2?
OXYLOG 2 is a medical device that received FDA 510(k) clearance on 1997-01-06. The listed applicant is P.K. Morgan , Ltd.. The 510(k) number is K954731.
When did OXYLOG 2 receive FDA 510(k) clearance?
OXYLOG 2 received FDA 510(k) clearance on 1997-01-06, under 510(k) number K954731.
Who is the listed applicant for OXYLOG 2?
The FDA 510(k) record lists P.K. Morgan , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OXYLOG 2?
The FDA product code for OXYLOG 2 is BZL.
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 P.K. Morgan , Ltd. 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: BZL)
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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