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FDA 510(k)

MEDI-TRACE 200, MEDI-TRACE 200-30

K-Number: K960968 · 1996-10-28

ApplicantGraphic Controls Corp.
Decision Date1996-10-28
Product CodeDRX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDI-TRACE 200, MEDI-TRACE 200-30 is the device name listed in this FDA 510(k) record. The listed applicant is Graphic Controls Corp.. It received FDA 510(k) clearance on 1996-10-28 under 510(k) number K960968. 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 MEDI-TRACE 200, MEDI-TRACE 200-30?

MEDI-TRACE 200, MEDI-TRACE 200-30 is a medical device that received FDA 510(k) clearance on 1996-10-28. The listed applicant is Graphic Controls Corp.. The 510(k) number is K960968.

When did MEDI-TRACE 200, MEDI-TRACE 200-30 receive FDA 510(k) clearance?

MEDI-TRACE 200, MEDI-TRACE 200-30 received FDA 510(k) clearance on 1996-10-28, under 510(k) number K960968.

Who is the listed applicant for MEDI-TRACE 200, MEDI-TRACE 200-30?

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

What is the FDA product code for MEDI-TRACE 200, MEDI-TRACE 200-30?

The FDA product code for MEDI-TRACE 200, MEDI-TRACE 200-30 is DRX.

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Other records listing Graphic Controls 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.

K981964MEDI-TRACE 4103 NEONATAL ELECTRODEK983287MEDI-TRACE 1610C COMBINATION DEFIBRILLATION, MONITORING AND PACING ELECTRODEK974730SOFTRANS PLUS INTRAUTERINE PRESSURE CATHETER SYSTEM (IUP 5000, SOFTRANS PLUS IUPC)K980857MEDI-TRACE 1310P COMBINATION DEFIBRILLATION, MONITORING & PACING ELECTRODEK972970MEDI-TRACE 1510M COMBINATION DEFIBRILLATION, MONITORING AND PACING ELECTRODEK964387POINT OF USE II SHARPS-A-GATOR

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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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