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FDA 510(k)

MEDIAID PULSE OXIMETER M30 AND M34

K-Number: K071610 · 2007-11-05

ApplicantMediaid, Inc.
Decision Date2007-11-05
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDIAID PULSE OXIMETER M30 AND M34 is the device name listed in this FDA 510(k) record. The listed applicant is Mediaid, Inc.. It received FDA 510(k) clearance on 2007-11-05 under 510(k) number K071610. 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 MEDIAID PULSE OXIMETER M30 AND M34?

MEDIAID PULSE OXIMETER M30 AND M34 is a medical device that received FDA 510(k) clearance on 2007-11-05. The listed applicant is Mediaid, Inc.. The 510(k) number is K071610.

When did MEDIAID PULSE OXIMETER M30 AND M34 receive FDA 510(k) clearance?

MEDIAID PULSE OXIMETER M30 AND M34 received FDA 510(k) clearance on 2007-11-05, under 510(k) number K071610.

Who is the listed applicant for MEDIAID PULSE OXIMETER M30 AND M34?

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

What is the FDA product code for MEDIAID PULSE OXIMETER M30 AND M34?

The FDA product code for MEDIAID PULSE OXIMETER M30 AND M34 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Mediaid, 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.

K071642MEDIAID M960 SERIES, VITAL SIGNS MONITOR AND MEDIAID M900 SERIES, PULSE OXIMETERK061896MEDIAID DISPOSABLE NON-ADHESIVE SENSORS, MODEL CST050-2101N; REUSABLE FINGER CLIP SP02 SENSORS, MODEL CST060-2101NK041964MEDIAID REUSABLE FINGER CLIP SPO2 SENSORS AND DISPOSABLE NON-ADHESIVE SENSORS AND ADHESIVE SPO2 SENSORS

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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