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FDA 510(k)

MULTITRAK-PLUS

K-Number: K930894 · 1993-11-01

ApplicantZymed Medical Instrumentation
Decision Date1993-11-01
Product CodeDSH
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MULTITRAK-PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Zymed Medical Instrumentation. It received FDA 510(k) clearance on 1993-11-01 under 510(k) number K930894. 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 MULTITRAK-PLUS?

MULTITRAK-PLUS is a medical device that received FDA 510(k) clearance on 1993-11-01. The listed applicant is Zymed Medical Instrumentation. The 510(k) number is K930894.

When did MULTITRAK-PLUS receive FDA 510(k) clearance?

MULTITRAK-PLUS received FDA 510(k) clearance on 1993-11-01, under 510(k) number K930894.

Who is the listed applicant for MULTITRAK-PLUS?

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

What is the FDA product code for MULTITRAK-PLUS?

The FDA product code for MULTITRAK-PLUS is DSH.

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Other records listing Zymed Medical Instrumentation 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.

K002004ZYBITK992197MODIFICATION TO ZYMED HOLTER 2000K990170HOLTER 2000K984089ZYMED TELEMETRY SYSTEM, MODEL EASI VIEWK955015ZYMED HOLTER SCANNER MODEL 2010K951370ZYMED TELEMETRY SYSTEM; MODEL T8010

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Related Devices (Code: DSH)

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.

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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