Cleared Traditional

K863045 - PROGRAMMER MODEL 2035/ELECTROGRAM CABLE...

K863045 is the FDA 510(k) clearance for PROGRAMMER MODEL 2035/ELECTROGRAM CABLE... by Cardiac Pacemakers, Inc.. It is a Class 3 Cardiovascular device (product code KRG) cleared through the Traditional 510(k) pathway after a 48-day FDA review.

K863045 · Cardiac Pacemakers, Inc. · Cardiovascular device
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Sep 1986
Decision
48d
Days
Class 3
Risk

K863045 is an FDA 510(k) clearance for the PROGRAMMER MODEL 2035/ELECTROGRAM CABLE MODEL 6580. Classified as Programmer, Pacemaker (product code KRG), Class III - Premarket Approval.

Submitted by Cardiac Pacemakers, Inc. (St. Paul, US). The FDA issued a Cleared decision on September 29, 1986 after a review of 48 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.3700 - the FDA cardiovascular device oversight framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: High-complexity regulatory submission. High regulatory complexity profile. This clearance follows a standard predicate-based equivalence path within the Cardiovascular review framework, consistent with the majority of Class II 510(k) submissions.

View all Cardiac Pacemakers, Inc. devices

Submission Details

510(k) Number K863045 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 12, 1986
Decision Date September 29, 1986
Days to Decision 48 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
77d faster than avg
Panel avg: 125d · This submission: 48d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code KRG Programmer, Pacemaker
Device Class Class 3 - Premarket Approval
CFR Regulation 21 CFR 870.3700
What this classification means

Class III devices typically require Premarket Approval (PMA) with clinical evidence. Clearance through 510(k) for Class III devices is granted only when substantial equivalence to a valid predicate can be established.

Regulatory Peers - KRG Programmer, Pacemaker

All 17
Devices cleared under the same product code (KRG) and FDA review panel - the closest regulatory comparables to K863045.
MODEL 1740 PERSONAL POCKET PROGRAMMER
K864712 · Telectronics, Inc. · Dec 1987
MODEL 5600B PROGRAMMER, PACEMAKER
K871986 · Telectronics, Inc. · Jun 1987
ULTRA SOFTWARE MODULE: MODEL 2016
K863046 · Cardiac Pacemakers, Inc. · Dec 1986
SOFTWARE MODULE/2035 PROG AND ASTRA/T PULSE GEN
K860584 · Cardiac Pacemakers, Inc. · Jun 1986
DIALOG PROGRAMMER 700 - PROGRAM VERSION 6.37
K860546 · Pacesetter Systems · Apr 1986
HANDHELD PACEMAKER PROGRAMMER & SOFTWAR
K842364 · Cardiac Pacemakers, Inc. · Sep 1984