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FDA 510(k)

SIEMENS SC9000/SC9015 TCP02/C02 MODULE

K-Number: K980287 · 1998-08-12

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1998-08-12
Product CodeKLK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SIEMENS SC9000/SC9015 TCP02/C02 MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 1998-08-12 under 510(k) number K980287. The device is classified under product code KLK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIEMENS SC9000/SC9015 TCP02/C02 MODULE?

SIEMENS SC9000/SC9015 TCP02/C02 MODULE is a medical device that received FDA 510(k) clearance on 1998-08-12. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K980287.

When did SIEMENS SC9000/SC9015 TCP02/C02 MODULE receive FDA 510(k) clearance?

SIEMENS SC9000/SC9015 TCP02/C02 MODULE received FDA 510(k) clearance on 1998-08-12, under 510(k) number K980287.

Who is the listed applicant for SIEMENS SC9000/SC9015 TCP02/C02 MODULE?

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

What is the FDA product code for SIEMENS SC9000/SC9015 TCP02/C02 MODULE?

The FDA product code for SIEMENS SC9000/SC9015 TCP02/C02 MODULE is KLK.

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Related Devices (Code: KLK)

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.

K003943MICROGAS 7650 TRANSCUTANEOUS MONITORLinde Medical Sensors AGK991644MICROGAS 7650 TRANSCUTANEOUS MONITORLinde Medical Sensors AGK924709SATCARE OXYGEN CONTROLLER/MONITOR W/ PULSE OXIMETEAir-Shields, Inc.K924679OXYCARE(TM) OXYGEN CONTROLLER/MONITORAir-Shields Vickers, Inc.K925910HEWLETT-PACKARD MODEL M1018A TCPO2/TOPCO2 MODULEHewlett-Packard Co.K893133HORIZON 2110/HORIZON 2210 264-XXX-XXX/261-XXX-XXXMennen Medical, Inc.

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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