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FDA 510(k)

MODIFICATION TO ONYX, FINGER CLIP PULSE OXIMETER, MODEL 9500

K-Number: K001085 · 2000-05-01

ApplicantNonin Medical, Inc.
Decision Date2000-05-01
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO ONYX, FINGER CLIP PULSE OXIMETER, MODEL 9500 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 2000-05-01 under 510(k) number K001085. 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 MODIFICATION TO ONYX, FINGER CLIP PULSE OXIMETER, MODEL 9500?

MODIFICATION TO ONYX, FINGER CLIP PULSE OXIMETER, MODEL 9500 is a medical device that received FDA 510(k) clearance on 2000-05-01. The listed applicant is Nonin Medical, Inc.. The 510(k) number is K001085.

When did MODIFICATION TO ONYX, FINGER CLIP PULSE OXIMETER, MODEL 9500 receive FDA 510(k) clearance?

MODIFICATION TO ONYX, FINGER CLIP PULSE OXIMETER, MODEL 9500 received FDA 510(k) clearance on 2000-05-01, under 510(k) number K001085.

Who is the listed applicant for MODIFICATION TO ONYX, FINGER CLIP PULSE OXIMETER, MODEL 9500?

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 MODIFICATION TO ONYX, FINGER CLIP PULSE OXIMETER, MODEL 9500?

The FDA product code for MODIFICATION TO ONYX, FINGER CLIP PULSE OXIMETER, MODEL 9500 is DQA.

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Other records listing Nonin Medical, Inc. as applicant

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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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