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FDA 510(k)

ADDITIONAL USE FOR ECG DISPOSABLE ELECTRODE V-PAD

K-Number: K864690 · 1987-05-06

ApplicantMulti Biosensors, Inc.
Decision Date1987-05-06
Product CodeDRX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ADDITIONAL USE FOR ECG DISPOSABLE ELECTRODE V-PAD is the device name listed in this FDA 510(k) record. The listed applicant is Multi Biosensors, Inc.. It received FDA 510(k) clearance on 1987-05-06 under 510(k) number K864690. The device is classified under product code DRX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADDITIONAL USE FOR ECG DISPOSABLE ELECTRODE V-PAD?

ADDITIONAL USE FOR ECG DISPOSABLE ELECTRODE V-PAD is a medical device that received FDA 510(k) clearance on 1987-05-06. The listed applicant is Multi Biosensors, Inc.. The 510(k) number is K864690.

When did ADDITIONAL USE FOR ECG DISPOSABLE ELECTRODE V-PAD receive FDA 510(k) clearance?

ADDITIONAL USE FOR ECG DISPOSABLE ELECTRODE V-PAD received FDA 510(k) clearance on 1987-05-06, under 510(k) number K864690.

Who is the listed applicant for ADDITIONAL USE FOR ECG DISPOSABLE ELECTRODE V-PAD?

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

What is the FDA product code for ADDITIONAL USE FOR ECG DISPOSABLE ELECTRODE V-PAD?

The FDA product code for ADDITIONAL USE FOR ECG DISPOSABLE ELECTRODE V-PAD is DRX.

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 Multi Biosensors, Inc. 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.

K842514ELECTROCARDIOGRAM DISPOS. ELECTRODE PAD

Related Devices (Code: DRX)

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.

K171244PhysiotraceNimbleheart, Inc.K123658BIOMODULE 3-M1Zephyr Technology CorporationK101576CENTERRIDGE DIAGNOSTIC ECG ELECTRODE, CENTERRIDGE MONITORING ECG ELECTRODESTeam Innovations, Inc.K101685IP-SETIntegral Process SasK100129AMBU BLUE SENSOR NEO, AMBU BLUE SENSOR NEO XAmbu A/SK093327INTCO TAB ELECTRODEShanghai Intco Electrode Manufacturing 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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