FDA 510(k)

MEDTRONIC #1992-2 DUAL RATE TRANSMITTER

K-Number: K820988 · 1982-06-23

Decision Date1982-06-23

Product CodeGZB

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

MEDTRONIC #1992-2 DUAL RATE TRANSMITTER is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1982-06-23 under 510(k) number K820988. The device is classified under product code GZB. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDTRONIC #1992-2 DUAL RATE TRANSMITTER?

MEDTRONIC #1992-2 DUAL RATE TRANSMITTER is a medical device that received FDA 510(k) clearance on 1982-06-23. The listed applicant is Medtronic Vascular. The 510(k) number is K820988.

When did MEDTRONIC #1992-2 DUAL RATE TRANSMITTER receive FDA 510(k) clearance?

MEDTRONIC #1992-2 DUAL RATE TRANSMITTER received FDA 510(k) clearance on 1982-06-23, under 510(k) number K820988.

Who is the listed applicant for MEDTRONIC #1992-2 DUAL RATE TRANSMITTER?

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 #1992-2 DUAL RATE TRANSMITTER?

The FDA product code for MEDTRONIC #1992-2 DUAL RATE TRANSMITTER is GZB.

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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.