MICRO SPAN TRANSCUTANEOUS OXYGEN MONIT
K-Number: K840918 · 1984-04-17
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Device Summary
Frequently Asked Questions
What is the MICRO SPAN TRANSCUTANEOUS OXYGEN MONIT?
MICRO SPAN TRANSCUTANEOUS OXYGEN MONIT is a medical device that received FDA 510(k) clearance on 1984-04-17. The listed applicant is Biochem International, Inc.. The 510(k) number is K840918.
When did MICRO SPAN TRANSCUTANEOUS OXYGEN MONIT receive FDA 510(k) clearance?
MICRO SPAN TRANSCUTANEOUS OXYGEN MONIT received FDA 510(k) clearance on 1984-04-17, under 510(k) number K840918.
Who is the listed applicant for MICRO SPAN TRANSCUTANEOUS OXYGEN MONIT?
The FDA 510(k) record lists Biochem International, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MICRO SPAN TRANSCUTANEOUS OXYGEN MONIT?
The FDA product code for MICRO SPAN TRANSCUTANEOUS OXYGEN MONIT is KLK.
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 Biochem International, 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: KLK)
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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