FDA 510(k)

MEDTRONIC MOD. 3852 STERIL-ICE ELECTRODE

K-Number: K792351 · 1979-12-05

Decision Date1979-12-05

Product CodeGXY

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

MEDTRONIC MOD. 3852 STERIL-ICE 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 1979-12-05 under 510(k) number K792351. The device is classified under product code GXY. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDTRONIC MOD. 3852 STERIL-ICE ELECTRODE?

MEDTRONIC MOD. 3852 STERIL-ICE ELECTRODE is a medical device that received FDA 510(k) clearance on 1979-12-05. The listed applicant is Medtronic Vascular. The 510(k) number is K792351.

When did MEDTRONIC MOD. 3852 STERIL-ICE ELECTRODE receive FDA 510(k) clearance?

MEDTRONIC MOD. 3852 STERIL-ICE ELECTRODE received FDA 510(k) clearance on 1979-12-05, under 510(k) number K792351.

Who is the listed applicant for MEDTRONIC MOD. 3852 STERIL-ICE 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 MEDTRONIC MOD. 3852 STERIL-ICE ELECTRODE?

The FDA product code for MEDTRONIC MOD. 3852 STERIL-ICE ELECTRODE is GXY.

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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.