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FDA 510(k)

MVM 4000 HOLTER IV RECORDER

K-Number: K853985 · 1985-11-06

ApplicantMountain View Medical
Decision Date1985-11-06
Product CodeDSH
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MVM 4000 HOLTER IV RECORDER is the device name listed in this FDA 510(k) record. The listed applicant is Mountain View Medical. It received FDA 510(k) clearance on 1985-11-06 under 510(k) number K853985. 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 MVM 4000 HOLTER IV RECORDER?

MVM 4000 HOLTER IV RECORDER is a medical device that received FDA 510(k) clearance on 1985-11-06. The listed applicant is Mountain View Medical. The 510(k) number is K853985.

When did MVM 4000 HOLTER IV RECORDER receive FDA 510(k) clearance?

MVM 4000 HOLTER IV RECORDER received FDA 510(k) clearance on 1985-11-06, under 510(k) number K853985.

Who is the listed applicant for MVM 4000 HOLTER IV RECORDER?

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

What is the FDA product code for MVM 4000 HOLTER IV RECORDER?

The FDA product code for MVM 4000 HOLTER IV RECORDER is DSH.

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 Mountain View Medical 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.

K861240BECHLER MEDICAL, MODEL 5000,THE WIZ HOLTER SCANNER

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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