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FDA 510(k)

PREGELLED DISPOSABLE E.K.G. ELECTRODE

K-Number: K781430 · 1978-10-31

ApplicantVermont Medical, Inc.
Decision Date1978-10-31
Product CodeDRX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PREGELLED DISPOSABLE E.K.G. ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Vermont Medical, Inc.. It received FDA 510(k) clearance on 1978-10-31 under 510(k) number K781430. 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 PREGELLED DISPOSABLE E.K.G. ELECTRODE?

PREGELLED DISPOSABLE E.K.G. ELECTRODE is a medical device that received FDA 510(k) clearance on 1978-10-31. The listed applicant is Vermont Medical, Inc.. The 510(k) number is K781430.

When did PREGELLED DISPOSABLE E.K.G. ELECTRODE receive FDA 510(k) clearance?

PREGELLED DISPOSABLE E.K.G. ELECTRODE received FDA 510(k) clearance on 1978-10-31, under 510(k) number K781430.

Who is the listed applicant for PREGELLED DISPOSABLE E.K.G. ELECTRODE?

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

What is the FDA product code for PREGELLED DISPOSABLE E.K.G. ELECTRODE?

The FDA product code for PREGELLED DISPOSABLE E.K.G. ELECTRODE is DRX.

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Other records listing Vermont Medical, 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.

K030073VERMED A10021 RESTING EKG TAB ELECTRODEK021537MULTIPURPOSE NEUROPLUS ELECTRODE, MODEL A10005K010638NEUROPLUS, MODEL A10040, A10041, A10042, A10043K921498VER MED A10011 PNS DUAL ELEMENT ELECTRODEK915831THERMAL PROBE COVERK911687VER-MED A10020 RESTING EKG ELECTRODE

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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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