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FDA 510(k)

CORDIS PACEMAKER PROGRAMMERS 255A & 256A

K-Number: K810552 · 1981-03-20

ApplicantCordis Corp.
Decision Date1981-03-20
Product CodeKRG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CORDIS PACEMAKER PROGRAMMERS 255A & 256A is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1981-03-20 under 510(k) number K810552. 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 CORDIS PACEMAKER PROGRAMMERS 255A & 256A?

CORDIS PACEMAKER PROGRAMMERS 255A & 256A is a medical device that received FDA 510(k) clearance on 1981-03-20. The listed applicant is Cordis Corp.. The 510(k) number is K810552.

When did CORDIS PACEMAKER PROGRAMMERS 255A & 256A receive FDA 510(k) clearance?

CORDIS PACEMAKER PROGRAMMERS 255A & 256A received FDA 510(k) clearance on 1981-03-20, under 510(k) number K810552.

Who is the listed applicant for CORDIS PACEMAKER PROGRAMMERS 255A & 256A?

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

What is the FDA product code for CORDIS PACEMAKER PROGRAMMERS 255A & 256A?

The FDA product code for CORDIS PACEMAKER PROGRAMMERS 255A & 256A is KRG.

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Other records listing Cordis Corp. 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.

K112797POWERFLEX PRO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY CATHETERK101651ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE, ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIREK082143MICRO GUIDE CATHETER XPK062798SMART NITINOL SELF-EXPANDING STENT, MODEL C06120MB, C07120MB, C08120MB, C06150MB, C07150MB, C08150MBK060877PALMAZ BLUE .014 TRANSHEPATIC BILIARY STENT SYSTEM-MODEL PB1550,BAS,BAX,PB1560,BAS,BAX,PB1850,BAS,BAXPB1860BAS,BAXK050645CORDIS AMIIA .014 PTA BALLOON CATHETER

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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.K880738MODEL 2331T PATIENT PROGRAMMERMedtronic VascularK882429MODEL 255A PROGRAMMER III, W/SOFTWARE REVI. 4004Tpl-Cordis, Inc.K864712MODEL 1740 PERSONAL POCKET PROGRAMMERTelectronics, Inc.K871986MODEL 5600B PROGRAMMER, PACEMAKERTelectronics, 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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