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FDA 510(k)

OXYSHUTTLE II ,MODIFICATION

K-Number: K925542 · 1993-02-17

ApplicantSensor Medics Corp.
Decision Date1993-02-17
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

OXYSHUTTLE II ,MODIFICATION is the device name listed in this FDA 510(k) record. The listed applicant is Sensor Medics Corp.. It received FDA 510(k) clearance on 1993-02-17 under 510(k) number K925542. 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 OXYSHUTTLE II ,MODIFICATION?

OXYSHUTTLE II ,MODIFICATION is a medical device that received FDA 510(k) clearance on 1993-02-17. The listed applicant is Sensor Medics Corp.. The 510(k) number is K925542.

When did OXYSHUTTLE II ,MODIFICATION receive FDA 510(k) clearance?

OXYSHUTTLE II ,MODIFICATION received FDA 510(k) clearance on 1993-02-17, under 510(k) number K925542.

Who is the listed applicant for OXYSHUTTLE II ,MODIFICATION?

The FDA 510(k) record lists Sensor Medics Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OXYSHUTTLE II ,MODIFICATION?

The FDA product code for OXYSHUTTLE II ,MODIFICATION is DQA.

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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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