Cleared Traditional

K854132 - COOK PACEMAKER 332T

K854132 is the FDA 510(k) clearance for COOK PACEMAKER 332T by Cook Pacemaker Corp.. It is a Class 3 Cardiovascular device (product code DXY) cleared through the Traditional 510(k) pathway after a 54-day FDA review.

K854132 · Cook Pacemaker Corp. · Cardiovascular device
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Dec 1985
Decision
54d
Days
Class 3
Risk

K854132 is an FDA 510(k) clearance for the COOK PACEMAKER 332T, SERIES R BIPOLAR CARDIAC PULS. Classified as Implantable Pacemaker Pulse-generator (product code DXY), Class III - Premarket Approval.

Submitted by Cook Pacemaker Corp. (Leechburg, US). The FDA issued a Cleared decision on December 3, 1985 after a review of 54 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.3610 - 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 Cook Pacemaker Corp. devices

Submission Details

510(k) Number K854132 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 10, 1985
Decision Date December 03, 1985
Days to Decision 54 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
71d faster than avg
Panel avg: 125d · This submission: 54d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code DXY Implantable Pacemaker Pulse-generator
Device Class Class 3 - Premarket Approval
CFR Regulation 21 CFR 870.3610
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 - DXY Implantable Pacemaker Pulse-generator

All 339
Devices cleared under the same product code (DXY) and FDA review panel - the closest regulatory comparables to K854132.
CORDIS MULTICOR ST, MODEL 350A
K851968 · Cordis Corp. · Jan 1986
PROGRAMALITH III MODELS 238 & 239
K854195 · Pacesetter Systems · Jan 1986
BIPOLAR CARDIAC PULSE GENERATOR WITH TELEMETRY
K854919 · Cook Pacemaker Corp. · Dec 1985
MULTICOR II 402B & 402C MULTIPROGRAM. CARDIAC PACE
K854214 · Cordis Corp. · Dec 1985
SUPRIMA MODEL 254-22
K852339 · Intermedics, Inc. · Nov 1985
SUPRIMA MODEL 254-24
K852340 · Intermedics, Inc. · Nov 1985