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FDA 510(k)

MODEL 255A PROGRAMMER III, W/SOFTWARE REVI. 4004

K-Number: K882429 · 1988-07-22

ApplicantTpl-Cordis, Inc.
Decision Date1988-07-22
Product CodeKRG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL 255A PROGRAMMER III, W/SOFTWARE REVI. 4004 is the device name listed in this FDA 510(k) record. The listed applicant is Tpl-Cordis, Inc.. It received FDA 510(k) clearance on 1988-07-22 under 510(k) number K882429. 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 255A PROGRAMMER III, W/SOFTWARE REVI. 4004?

MODEL 255A PROGRAMMER III, W/SOFTWARE REVI. 4004 is a medical device that received FDA 510(k) clearance on 1988-07-22. The listed applicant is Tpl-Cordis, Inc.. The 510(k) number is K882429.

When did MODEL 255A PROGRAMMER III, W/SOFTWARE REVI. 4004 receive FDA 510(k) clearance?

MODEL 255A PROGRAMMER III, W/SOFTWARE REVI. 4004 received FDA 510(k) clearance on 1988-07-22, under 510(k) number K882429.

Who is the listed applicant for MODEL 255A PROGRAMMER III, W/SOFTWARE REVI. 4004?

The FDA 510(k) record lists Tpl-Cordis, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL 255A PROGRAMMER III, W/SOFTWARE REVI. 4004?

The FDA product code for MODEL 255A PROGRAMMER III, W/SOFTWARE REVI. 4004 is KRG.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Tpl-Cordis, Inc. as applicant

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.

K885240MODIFIED ANCOR & HI-FLEX UNIPOLAR ACTIVE FIX. LEADK880898MULTICOR AND PACEMAKERSK880432VICOR PACER, MODEL 410AK873158MODIFIED MULTICOR AND OMNI-STANICOR PACEMAKERSK873202VICOR, MODEL 410A

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.K880738MODEL 2331T PATIENT PROGRAMMERMedtronic VascularK864712MODEL 1740 PERSONAL POCKET PROGRAMMERTelectronics, Inc.K871986MODEL 5600B PROGRAMMER, PACEMAKERTelectronics, Inc.K863046ULTRA SOFTWARE MODULE: MODEL 2016Cardiac Pacemakers, Inc.

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.

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