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FDA 510(k)

MINI OX III OXYGEN MONITOR

K-Number: K833326 · 1983-11-03

ApplicantCatalyst Research Corp.
Decision Date1983-11-03
Product CodeBXL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MINI OX III OXYGEN MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Catalyst Research Corp.. It received FDA 510(k) clearance on 1983-11-03 under 510(k) number K833326. The device is classified under product code BXL. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINI OX III OXYGEN MONITOR?

MINI OX III OXYGEN MONITOR is a medical device that received FDA 510(k) clearance on 1983-11-03. The listed applicant is Catalyst Research Corp.. The 510(k) number is K833326.

When did MINI OX III OXYGEN MONITOR receive FDA 510(k) clearance?

MINI OX III OXYGEN MONITOR received FDA 510(k) clearance on 1983-11-03, under 510(k) number K833326.

Who is the listed applicant for MINI OX III OXYGEN MONITOR?

The FDA 510(k) record lists Catalyst Research Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MINI OX III OXYGEN MONITOR?

The FDA product code for MINI OX III OXYGEN MONITOR is BXL.

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Other records listing Catalyst Research Corp. 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.

K905310MINIOX V PULSE OXIMETERK874132MINIOX IV PORTABLE PULSE OXIMETERK862798MINIOX 100 PULSE OXIMETERK833995MINI OX IIK790785MODEL M25RL, (CRC) OXYGEN ANALYZERK790784MODEL M25R, OXYGEN ANALYZER

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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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