Omnicor Programmer Model 222C

FDA 510(k) K791419 · Cordis Corp.

Substantially Equivalent

510(k) numberK791419

Submission

Device name
Omnicor Programmer Model 222C
Applicant
Cordis Corp.
Mchenry, IL, US
Received
July 17, 1979
Decision date
November 27, 1979
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KRG – Programmer, Pacemaker
Device class
Class III (high risk)
Regulation
21 CFR 870.3700
Specialty
Cardiovascular

Other 510(k)s with product code KRG

510(k)DeviceApplicantDecision
K933278Intermedics Triangle Chest Probe Model 526-04KRG · Traditional Intermedics, Inc.03/15/1995SE
K884522Model 5650 Optimate Personal ProgrammerKRG · Traditional Teletronics, Inc.08/25/1989SE
K880738Model 2331T Patient ProgrammerKRG · Traditional Medtronic Vascular11/17/1988SE
K882429Model 255A Programmer III, W/Software Revi. 4004KRG · Traditional Tpl-Cordis, Inc.07/22/1988SE
K864712Model 1740 Personal Pocket ProgrammerKRG · Traditional Telectronics, Inc.12/17/1987SE
K871986Model 5600B Programmer, PacemakerKRG · Traditional Telectronics, Inc.06/24/1987SE
K863046Ultra Software Module: Model 2016KRG · Traditional Cardiac Pacemakers, Inc.12/05/1986SE
K863045Programmer Model 2035/ELECTROGRAM Cable Model 6580KRG · Traditional Cardiac Pacemakers, Inc.09/29/1986SE
K860584Software MODULE/2035 Prog and Astra/T Pulse GenKRG · Traditional Cardiac Pacemakers, Inc.06/06/1986SE
K860546Dialog Programmer 700 - Program Version 6.37KRG · Traditional Pacesetter Systems04/23/1986SE

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Questions and answers

When was Omnicor Programmer Model 222C cleared by the FDA?

Omnicor Programmer Model 222C (K791419) received a 510(k) decision of Substantially Equivalent on November 27, 1979, 133 days after the submission was received.

What is the product code of K791419?

The FDA product code is KRG – Programmer, Pacemaker, a Class III (high risk) device regulated under 21 CFR 870.3700.