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FDA 510(k)

MODIFIED MODEL 9431 TELETRACE TRANSMITTER

K-Number: K872246 · 1987-07-21

ApplicantMedtronic Vascular
Decision Date1987-07-21
Product CodeDSH
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODIFIED MODEL 9431 TELETRACE TRANSMITTER is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1987-07-21 under 510(k) number K872246. The device is classified under product code DSH. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED MODEL 9431 TELETRACE TRANSMITTER?

MODIFIED MODEL 9431 TELETRACE TRANSMITTER is a medical device that received FDA 510(k) clearance on 1987-07-21. The listed applicant is Medtronic Vascular. The 510(k) number is K872246.

When did MODIFIED MODEL 9431 TELETRACE TRANSMITTER receive FDA 510(k) clearance?

MODIFIED MODEL 9431 TELETRACE TRANSMITTER received FDA 510(k) clearance on 1987-07-21, under 510(k) number K872246.

Who is the listed applicant for MODIFIED MODEL 9431 TELETRACE TRANSMITTER?

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

What is the FDA product code for MODIFIED MODEL 9431 TELETRACE TRANSMITTER?

The FDA product code for MODIFIED MODEL 9431 TELETRACE TRANSMITTER is DSH.

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Related Devices (Code: DSH)

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K260157LifeLens Physiological MonitorLifeLens Technologies, Inc.K252389Rhythm Master ECG Patch (HM-15BB-AX, HM-15BW-AX, HM-15BW-DX)Smwmed, Inc.K253293VitaloJAK Clinic (Model 7100)Vitalograph , Ltd.K243650Zio® monitor (DFG0001)iRhythm Technologies, Inc.K243603AeviceMDAevice Health Pte. , Ltd.K242583AT-Patch (ATP-C130/ATP-C70)Atsens 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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