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FDA 510(k)

SIEMENS SAO2 + PULS OXIMETRY CARTRIDGE

K-Number: K893470 · 1989-08-03

ApplicantSiemens Medical Electronics
Decision Date1989-08-03
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SIEMENS SAO2 + PULS OXIMETRY CARTRIDGE is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Electronics. It received FDA 510(k) clearance on 1989-08-03 under 510(k) number K893470. 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 SIEMENS SAO2 + PULS OXIMETRY CARTRIDGE?

SIEMENS SAO2 + PULS OXIMETRY CARTRIDGE is a medical device that received FDA 510(k) clearance on 1989-08-03. The listed applicant is Siemens Medical Electronics. The 510(k) number is K893470.

When did SIEMENS SAO2 + PULS OXIMETRY CARTRIDGE receive FDA 510(k) clearance?

SIEMENS SAO2 + PULS OXIMETRY CARTRIDGE received FDA 510(k) clearance on 1989-08-03, under 510(k) number K893470.

Who is the listed applicant for SIEMENS SAO2 + PULS OXIMETRY CARTRIDGE?

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

What is the FDA product code for SIEMENS SAO2 + PULS OXIMETRY CARTRIDGE?

The FDA product code for SIEMENS SAO2 + PULS OXIMETRY CARTRIDGE is DQA.

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Other records listing Siemens Medical Electronics 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.

K935043SIEMENS CLINICAL WORK STATIONK921930SIEMENS SIRECUST 700 BEDSIDES/ACCESSORIES, MODIFIK920445SIEMENS SIRECUST PENTA SYSTEM AND ACCESSORIESK914765SIEMENS NP NONINVASIVE BLOOD PRESS MEASUREMENT SYSK912070SIEMENS RADIOTOM 904 & 904E ELECTROSURGERY UNITK913489SIEMENS MICRO2 PULSE OXIMETER

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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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