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FDA 510(k)

MINOLTA PULSOX-3SI, PULSOX-3IA, PULSOX-3LI

K-Number: K010413 · 2001-08-02

ApplicantKonica Minolta Sensing, Inc.
Decision Date2001-08-02
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MINOLTA PULSOX-3SI, PULSOX-3IA, PULSOX-3LI is the device name listed in this FDA 510(k) record. The listed applicant is Konica Minolta Sensing, Inc.. It received FDA 510(k) clearance on 2001-08-02 under 510(k) number K010413. 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 MINOLTA PULSOX-3SI, PULSOX-3IA, PULSOX-3LI?

MINOLTA PULSOX-3SI, PULSOX-3IA, PULSOX-3LI is a medical device that received FDA 510(k) clearance on 2001-08-02. The listed applicant is Konica Minolta Sensing, Inc.. The 510(k) number is K010413.

When did MINOLTA PULSOX-3SI, PULSOX-3IA, PULSOX-3LI receive FDA 510(k) clearance?

MINOLTA PULSOX-3SI, PULSOX-3IA, PULSOX-3LI received FDA 510(k) clearance on 2001-08-02, under 510(k) number K010413.

Who is the listed applicant for MINOLTA PULSOX-3SI, PULSOX-3IA, PULSOX-3LI?

The FDA 510(k) record lists Konica Minolta Sensing, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MINOLTA PULSOX-3SI, PULSOX-3IA, PULSOX-3LI?

The FDA product code for MINOLTA PULSOX-3SI, PULSOX-3IA, PULSOX-3LI is DQA.

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.

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Other records listing Konica Minolta Sensing, 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.

K053419KONICA MINOLTA PULSOX-300, 300IK021469MINOLTA PULSOX-2

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

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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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