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FDA 510(k)

RADIOLUCENT ECG ELECTRODE MODEL NO: 1680

K-Number: K890201 · 1989-03-15

ApplicantMedtronic Vascular
Decision Date1989-03-15
Product CodeDRX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RADIOLUCENT ECG ELECTRODE MODEL NO: 1680 is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1989-03-15 under 510(k) number K890201. 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 RADIOLUCENT ECG ELECTRODE MODEL NO: 1680?

RADIOLUCENT ECG ELECTRODE MODEL NO: 1680 is a medical device that received FDA 510(k) clearance on 1989-03-15. The listed applicant is Medtronic Vascular. The 510(k) number is K890201.

When did RADIOLUCENT ECG ELECTRODE MODEL NO: 1680 receive FDA 510(k) clearance?

RADIOLUCENT ECG ELECTRODE MODEL NO: 1680 received FDA 510(k) clearance on 1989-03-15, under 510(k) number K890201.

Who is the listed applicant for RADIOLUCENT ECG ELECTRODE MODEL NO: 1680?

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

What is the FDA product code for RADIOLUCENT ECG ELECTRODE MODEL NO: 1680?

The FDA product code for RADIOLUCENT ECG ELECTRODE MODEL NO: 1680 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.

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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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