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FDA 510(k)

MODEL MSC SA02-5000 PULSE OXIMETER

K-Number: K902192 · 1990-08-23

ApplicantMedical Systems Corp.
Decision Date1990-08-23
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL MSC SA02-5000 PULSE OXIMETER is the device name listed in this FDA 510(k) record. The listed applicant is Medical Systems Corp.. It received FDA 510(k) clearance on 1990-08-23 under 510(k) number K902192. 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 MODEL MSC SA02-5000 PULSE OXIMETER?

MODEL MSC SA02-5000 PULSE OXIMETER is a medical device that received FDA 510(k) clearance on 1990-08-23. The listed applicant is Medical Systems Corp.. The 510(k) number is K902192.

When did MODEL MSC SA02-5000 PULSE OXIMETER receive FDA 510(k) clearance?

MODEL MSC SA02-5000 PULSE OXIMETER received FDA 510(k) clearance on 1990-08-23, under 510(k) number K902192.

Who is the listed applicant for MODEL MSC SA02-5000 PULSE OXIMETER?

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

What is the FDA product code for MODEL MSC SA02-5000 PULSE OXIMETER?

The FDA product code for MODEL MSC SA02-5000 PULSE OXIMETER 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 Medical Systems Corp. 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.

K931736M-FLEX 5000 C3PMDK921513SPIROLITE MODEL MSC-201 SPIROMETERK921485LA MONT VIDEO PATIENT MONITORING SYSTEMK904353CARDIOMATIC MODEL MSC-2001K903501RADIANT TEMPERATUR INDICATOR MODEL 25EK902608CARDIOMATIC MODEL MSC-1001

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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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