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FDA 510(k)

MINIOX IV PORTABLE PULSE OXIMETER

K-Number: K874132 · 1988-01-19

ApplicantCatalyst Research Corp.
Decision Date1988-01-19
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MINIOX IV PORTABLE PULSE OXIMETER 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 1988-01-19 under 510(k) number K874132. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINIOX IV PORTABLE PULSE OXIMETER?

MINIOX IV PORTABLE PULSE OXIMETER is a medical device that received FDA 510(k) clearance on 1988-01-19. The listed applicant is Catalyst Research Corp.. The 510(k) number is K874132.

When did MINIOX IV PORTABLE PULSE OXIMETER receive FDA 510(k) clearance?

MINIOX IV PORTABLE PULSE OXIMETER received FDA 510(k) clearance on 1988-01-19, under 510(k) number K874132.

Who is the listed applicant for MINIOX IV PORTABLE PULSE OXIMETER?

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 MINIOX IV PORTABLE PULSE OXIMETER?

The FDA product code for MINIOX IV PORTABLE PULSE OXIMETER is DQA.

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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 OXIMETERK862798MINIOX 100 PULSE OXIMETERK833995MINI OX IIK833326MINI OX III OXYGEN MONITORK790785MODEL M25RL, (CRC) OXYGEN ANALYZERK790784MODEL M25R, OXYGEN ANALYZER

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Related Devices (Code: DQA)

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.

K252821Reusable Adult SpO2 Clip Sensor (3m) (M1196A); Reusable Adult SpO2 Clip Sensor (0.9m) (M1196T)Philips Medizin Systeme Böblingen GmbHK252655Pulse Oximeter (PO-A2AO, PO-A2AT, PO-A3AO, PO-H1AO, PO-B1AO, PO-C5AO, PO-C5AT, PO-C6AO, PO-C6AT)Shenzhen Imdk Medical Technology Co., Ltd.K253887Nasal Alar SpO2 Sensor (989803205381); Nasal Alar SpO2 Sensor (989803205391); Nasal Alar Sp02 Sensor (989803205401)Philips Medizin SystemeK260931Unimed Reusable Finger Clip SpO2 Sensors (U403-49R and U103-49R)Unimed Medical Supplies, Inc.K252448AViTA Pulse Oximeter (SP61)Avita CorporationK252805YUWELL® Finger Pulse Oximeter (YX105, YX106, YX110, YX310)Jiangsu Yuyue Medical Equipment & Supply Co., Ltd.

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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