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FDA 510(k)

4100 PATIENT OXIMETER MODULE

K-Number: K043359 · 2005-01-07

ApplicantNonin Medical, Inc.
Decision Date2005-01-07
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

4100 PATIENT OXIMETER MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Nonin Medical, Inc.. It received FDA 510(k) clearance on 2005-01-07 under 510(k) number K043359. 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 4100 PATIENT OXIMETER MODULE?

4100 PATIENT OXIMETER MODULE is a medical device that received FDA 510(k) clearance on 2005-01-07. The listed applicant is Nonin Medical, Inc.. The 510(k) number is K043359.

When did 4100 PATIENT OXIMETER MODULE receive FDA 510(k) clearance?

4100 PATIENT OXIMETER MODULE received FDA 510(k) clearance on 2005-01-07, under 510(k) number K043359.

Who is the listed applicant for 4100 PATIENT OXIMETER MODULE?

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

What is the FDA product code for 4100 PATIENT OXIMETER MODULE?

The FDA product code for 4100 PATIENT OXIMETER MODULE is DQA.

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Other records listing Nonin Medical, Inc. as applicant

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K211498Nonin OTC Pulse Oximeter Model 3250K192900H500 Multi-Sensing Oximetry SystemK191403Pulse OximeterK190560SenSmart Model 8006CA Reusable Regional Oximetry Sensor, SenSmart Model 8006PI Disposable Patient InterfaceK172625Reusable, Finger Clip Nonin Medical CO-Met Oximetry SensorK160231Model X-100C CO-Met™ Oximetry System

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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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