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FDA 510(k)

HBO CABLE ASSEMBLY, RADIOMETER TC-02

K-Number: K905225 · 1991-04-10

ApplicantSechrist
Decision Date1991-04-10
Product CodeLKD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

HBO CABLE ASSEMBLY, RADIOMETER TC-02 is the device name listed in this FDA 510(k) record. The listed applicant is Sechrist. It received FDA 510(k) clearance on 1991-04-10 under 510(k) number K905225. The device is classified under product code LKD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HBO CABLE ASSEMBLY, RADIOMETER TC-02?

HBO CABLE ASSEMBLY, RADIOMETER TC-02 is a medical device that received FDA 510(k) clearance on 1991-04-10. The listed applicant is Sechrist. The 510(k) number is K905225.

When did HBO CABLE ASSEMBLY, RADIOMETER TC-02 receive FDA 510(k) clearance?

HBO CABLE ASSEMBLY, RADIOMETER TC-02 received FDA 510(k) clearance on 1991-04-10, under 510(k) number K905225.

Who is the listed applicant for HBO CABLE ASSEMBLY, RADIOMETER TC-02?

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

What is the FDA product code for HBO CABLE ASSEMBLY, RADIOMETER TC-02?

The FDA product code for HBO CABLE ASSEMBLY, RADIOMETER TC-02 is LKD.

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 Sechrist 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.

K920121SECHRIST IV-100B SAVI SYSTEM

Related Devices (Code: LKD)

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.

K232516Sentec Digital Monitoring System (SDMS) tCOM+Sentec AGK131253PERIFLUX 6000Perimed ABK110474PHILIPS INTELLIVUE TCG10Philips Medizinsysteme Boeblingen GmbH, Cardiac ANK101690SENTEC DIGITAL MONITOR, V-SIGN SENSOR AND V-SIGN SENSOR 2 WITH DIGITAL SENSOR ADAPER CABLESentec AGK093154TCM TOSCA MONITORING SYSTEM, TCM COMBIM MONITORING SYSTEMRadiometer Medical ApsK043357TOSCA 500 PCO2, SPO2 AND PULSE RATE MONITORING SYSTEM, MODEL 5202009Linde Medical Sensors AG

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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