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FDA 510(k)

TENDER-TRODE PREWIRED PEDIATRIC ECG ELECTRODE

K-Number: K090180 · 2009-06-17

ApplicantVermed, Inc.
Decision Date2009-06-17
Product CodeDRX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TENDER-TRODE PREWIRED PEDIATRIC ECG ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Vermed, Inc.. It received FDA 510(k) clearance on 2009-06-17 under 510(k) number K090180. 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 TENDER-TRODE PREWIRED PEDIATRIC ECG ELECTRODE?

TENDER-TRODE PREWIRED PEDIATRIC ECG ELECTRODE is a medical device that received FDA 510(k) clearance on 2009-06-17. The listed applicant is Vermed, Inc.. The 510(k) number is K090180.

When did TENDER-TRODE PREWIRED PEDIATRIC ECG ELECTRODE receive FDA 510(k) clearance?

TENDER-TRODE PREWIRED PEDIATRIC ECG ELECTRODE received FDA 510(k) clearance on 2009-06-17, under 510(k) number K090180.

Who is the listed applicant for TENDER-TRODE PREWIRED PEDIATRIC ECG ELECTRODE?

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

What is the FDA product code for TENDER-TRODE PREWIRED PEDIATRIC ECG ELECTRODE?

The FDA product code for TENDER-TRODE PREWIRED PEDIATRIC ECG ELECTRODE is DRX.

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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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