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FDA 510(k)

MODEL 1850 ELECTRODE

K-Number: K903918 · 1990-10-31

ApplicantMedtronic Vascular
Decision Date1990-10-31
Product CodeDRX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL 1850 ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1990-10-31 under 510(k) number K903918. 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 MODEL 1850 ELECTRODE?

MODEL 1850 ELECTRODE is a medical device that received FDA 510(k) clearance on 1990-10-31. The listed applicant is Medtronic Vascular. The 510(k) number is K903918.

When did MODEL 1850 ELECTRODE receive FDA 510(k) clearance?

MODEL 1850 ELECTRODE received FDA 510(k) clearance on 1990-10-31, under 510(k) number K903918.

Who is the listed applicant for MODEL 1850 ELECTRODE?

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 MODEL 1850 ELECTRODE?

The FDA product code for MODEL 1850 ELECTRODE is DRX.

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Other records listing Medtronic Vascular as applicant

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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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