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FDA 510(k)

DX SERIES FINGER SENSOR

K-Number: K100020 · 2010-03-08

ApplicantDixtal Medical, Inc.
Decision Date2010-03-08
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DX SERIES FINGER SENSOR is the device name listed in this FDA 510(k) record. The listed applicant is Dixtal Medical, Inc.. It received FDA 510(k) clearance on 2010-03-08 under 510(k) number K100020. 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 DX SERIES FINGER SENSOR?

DX SERIES FINGER SENSOR is a medical device that received FDA 510(k) clearance on 2010-03-08. The listed applicant is Dixtal Medical, Inc.. The 510(k) number is K100020.

When did DX SERIES FINGER SENSOR receive FDA 510(k) clearance?

DX SERIES FINGER SENSOR received FDA 510(k) clearance on 2010-03-08, under 510(k) number K100020.

Who is the listed applicant for DX SERIES FINGER SENSOR?

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

What is the FDA product code for DX SERIES FINGER SENSOR?

The FDA product code for DX SERIES FINGER SENSOR 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 Dixtal Medical, 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.

K103285DIXTAL DZ-4100 SERIES PULSE OXIMETER

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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