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FDA 510(k)

MODEL 2331T PATIENT PROGRAMMER

K-Number: K880738 · 1988-11-17

ApplicantMedtronic Vascular
Decision Date1988-11-17
Product CodeKRG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL 2331T PATIENT PROGRAMMER is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1988-11-17 under 510(k) number K880738. The device is classified under product code KRG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 2331T PATIENT PROGRAMMER?

MODEL 2331T PATIENT PROGRAMMER is a medical device that received FDA 510(k) clearance on 1988-11-17. The listed applicant is Medtronic Vascular. The 510(k) number is K880738.

When did MODEL 2331T PATIENT PROGRAMMER receive FDA 510(k) clearance?

MODEL 2331T PATIENT PROGRAMMER received FDA 510(k) clearance on 1988-11-17, under 510(k) number K880738.

Who is the listed applicant for MODEL 2331T PATIENT PROGRAMMER?

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 2331T PATIENT PROGRAMMER?

The FDA product code for MODEL 2331T PATIENT PROGRAMMER is KRG.

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Other records listing Medtronic Vascular as applicant

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Related Devices (Code: KRG)

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.

K933278INTERMEDICS TRIANGLE CHEST PROBE MODEL 526-04Intermedics, Inc.K884522MODEL 5650 OPTIMATE PERSONAL PROGRAMMERTeletronics, Inc.K882429MODEL 255A PROGRAMMER III, W/SOFTWARE REVI. 4004Tpl-Cordis, Inc.K864712MODEL 1740 PERSONAL POCKET PROGRAMMERTelectronics, Inc.K871986MODEL 5600B PROGRAMMER, PACEMAKERTelectronics, Inc.K863046ULTRA SOFTWARE MODULE: MODEL 2016Cardiac Pacemakers, Inc.

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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