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FDA 510(k)

E.S.O. (ELECTRO SENSOR OXI)

K-Number: K102442 · 2010-09-10

ApplicantLd Technology, LLC
Decision Date2010-09-10
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

E.S.O. (ELECTRO SENSOR OXI) is the device name listed in this FDA 510(k) record. The listed applicant is Ld Technology, LLC. It received FDA 510(k) clearance on 2010-09-10 under 510(k) number K102442. 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 E.S.O. (ELECTRO SENSOR OXI)?

E.S.O. (ELECTRO SENSOR OXI) is a medical device that received FDA 510(k) clearance on 2010-09-10. The listed applicant is Ld Technology, LLC. The 510(k) number is K102442.

When did E.S.O. (ELECTRO SENSOR OXI) receive FDA 510(k) clearance?

E.S.O. (ELECTRO SENSOR OXI) received FDA 510(k) clearance on 2010-09-10, under 510(k) number K102442.

Who is the listed applicant for E.S.O. (ELECTRO SENSOR OXI)?

The FDA 510(k) record lists Ld Technology, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for E.S.O. (ELECTRO SENSOR OXI)?

The FDA product code for E.S.O. (ELECTRO SENSOR OXI) is DQA.

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Other records listing Ld Technology, LLC 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.

K200287BP-BT KioskK200141Oxi-W SystemK173696TBL-ABI SystemK160956LD-Oxi systemK131568SUDO PATHK130056PATIENT MONITOR

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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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