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FDA 510(k)

MICRO SPAN TRANSCUTANEOUS OXYGEN MONIT

K-Number: K840918 · 1984-04-17

Decision Date1984-04-17
Product CodeKLK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MICRO SPAN TRANSCUTANEOUS OXYGEN MONIT is the device name listed in this FDA 510(k) record. The listed applicant is Biochem International, Inc.. It received FDA 510(k) clearance on 1984-04-17 under 510(k) number K840918. The device is classified under product code KLK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

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.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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