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FDA 510(k)

OMNICOR PROGRAMMER MODEL 222C

K-Number: K791419 · 1979-11-27

ApplicantCordis Corp.
Decision Date1979-11-27
Product CodeKRG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

OMNICOR PROGRAMMER MODEL 222C is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1979-11-27 under 510(k) number K791419. 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 OMNICOR PROGRAMMER MODEL 222C?

OMNICOR PROGRAMMER MODEL 222C is a medical device that received FDA 510(k) clearance on 1979-11-27. The listed applicant is Cordis Corp.. The 510(k) number is K791419.

When did OMNICOR PROGRAMMER MODEL 222C receive FDA 510(k) clearance?

OMNICOR PROGRAMMER MODEL 222C received FDA 510(k) clearance on 1979-11-27, under 510(k) number K791419.

Who is the listed applicant for OMNICOR PROGRAMMER MODEL 222C?

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 OMNICOR PROGRAMMER MODEL 222C?

The FDA product code for OMNICOR PROGRAMMER MODEL 222C 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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