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FDA 510(k)

TRACET T-6000

K-Number: K930258 · 1993-04-16

ApplicantLectec Corp.
Decision Date1993-04-16
Product CodeDRX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TRACET T-6000 is the device name listed in this FDA 510(k) record. The listed applicant is Lectec Corp.. It received FDA 510(k) clearance on 1993-04-16 under 510(k) number K930258. 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 TRACET T-6000?

TRACET T-6000 is a medical device that received FDA 510(k) clearance on 1993-04-16. The listed applicant is Lectec Corp.. The 510(k) number is K930258.

When did TRACET T-6000 receive FDA 510(k) clearance?

TRACET T-6000 received FDA 510(k) clearance on 1993-04-16, under 510(k) number K930258.

Who is the listed applicant for TRACET T-6000?

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

What is the FDA product code for TRACET T-6000?

The FDA product code for TRACET T-6000 is DRX.

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Other records listing Lectec 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.

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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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