Cleared Traditional

K870909 - PACEMAKER FUNCTION ANALYZER

K870909 is an FDA 510(k) clearance for PACEMAKER FUNCTION ANALYZER, manufactured by Paceart, Inc.. The device is a Class 2 Cardiovascular device with product code KRE cleared through the Traditional 510(k) pathway after a 53-day FDA review.

K870909 · Paceart, Inc. · Cardiovascular device
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Apr 1987
Decision
53d
Days
Class 2
Risk

K870909 is an FDA 510(k) clearance for the PACEMAKER FUNCTION ANALYZER. Classified as Analyzer, Pacemaker Generator Function, Indirect (product code KRE), Class II - Special Controls.

Submitted by Paceart, Inc. (Millburn, US). The FDA issued a Cleared decision on April 27, 1987 after a review of 53 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.3640 - 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Paceart, Inc. devices

FDA 510(k) Submission Details - K870909

510(k) Number K870909 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 05, 1987
Decision Date April 27, 1987
Days to Decision 53 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
72d faster than avg
Panel avg: 125d · This submission: 53d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KRE Device Classification - Class 2, Special Controls

Product Code KRE Analyzer, Pacemaker Generator Function, Indirect
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.3640
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Cardiovascular devices follow this clearance model.

Regulatory Peers - KRE Analyzer, Pacemaker Generator Function, Indirect

All 7
Devices cleared under the same product code (KRE) and FDA review panel - the closest regulatory comparables to K870909.
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PACEMAKER SYS. ANALYZER 378
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CARDIOMEMO
K803286 · Instromedix, Inc. · Mar 1981