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FDA 510(k)

MEDI-TRACE 3600 SERIES OF ECG MONITORING ELECTRODE

K-Number: K963038 · 1996-11-15

Decision Date1996-11-15
Product CodeDRX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDI-TRACE 3600 SERIES OF ECG MONITORING ELECTRODE 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 1996-11-15 under 510(k) number K963038. 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 3600 SERIES OF ECG MONITORING ELECTRODE?

MEDI-TRACE 3600 SERIES OF ECG MONITORING ELECTRODE is a medical device that received FDA 510(k) clearance on 1996-11-15. The listed applicant is Graphic Controls Corp.. The 510(k) number is K963038.

When did MEDI-TRACE 3600 SERIES OF ECG MONITORING ELECTRODE receive FDA 510(k) clearance?

MEDI-TRACE 3600 SERIES OF ECG MONITORING ELECTRODE received FDA 510(k) clearance on 1996-11-15, under 510(k) number K963038.

Who is the listed applicant for MEDI-TRACE 3600 SERIES OF ECG MONITORING ELECTRODE?

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 3600 SERIES OF ECG MONITORING ELECTRODE?

The FDA product code for MEDI-TRACE 3600 SERIES OF ECG MONITORING ELECTRODE 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.

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.

View all 55 devices →

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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