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FDA 510(k)

SECURATRODE

K-Number: K874562 · 1988-01-28

ApplicantMeddev International Corp.
Decision Date1988-01-28
Product CodeDRX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SECURATRODE is the device name listed in this FDA 510(k) record. The listed applicant is Meddev International Corp.. It received FDA 510(k) clearance on 1988-01-28 under 510(k) number K874562. 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 SECURATRODE?

SECURATRODE is a medical device that received FDA 510(k) clearance on 1988-01-28. The listed applicant is Meddev International Corp.. The 510(k) number is K874562.

When did SECURATRODE receive FDA 510(k) clearance?

SECURATRODE received FDA 510(k) clearance on 1988-01-28, under 510(k) number K874562.

Who is the listed applicant for SECURATRODE?

The FDA 510(k) record lists Meddev International Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SECURATRODE?

The FDA product code for SECURATRODE 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 Meddev International Corp. 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.

K940284MEDDEV MULTARRAY MEDICAL EXAMINING LIGHT MODIFICATIONK931197MEDDEV MULTARRAY (TM) MEDICAL EXAMINATION LIGHTK771435URINARY LEG BAG, STEOILE

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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