Cleared Traditional

K820356 - MULTICOR (GAMMA) 402 CARDIAC PACER

K820356 is an FDA 510(k) clearance for MULTICOR (GAMMA) 402 CARDIAC PACER, manufactured by Cordis Corp.. The device is a Class 3 Cardiovascular device with product code DXY cleared through the Traditional 510(k) pathway after a 38-day FDA review.

K820356 · Cordis Corp. · Cardiovascular device
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Mar 1982
Decision
38d
Days
Class 3
Risk

K820356 is an FDA 510(k) clearance for the MULTICOR (GAMMA) 402 CARDIAC PACER. Classified as Implantable Pacemaker Pulse-generator (product code DXY), Class III - Premarket Approval.

Submitted by Cordis Corp. (Mchenry, US). The FDA issued a Cleared decision on March 18, 1982 after a review of 38 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 Cordis Corp. devices

FDA 510(k) Submission Details - K820356

510(k) Number K820356 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 08, 1982
Decision Date March 18, 1982
Days to Decision 38 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
87d faster than avg
Panel avg: 125d · This submission: 38d
Pathway characteristics
Predicate-based equivalence.

DXY Device Classification - Class 3, Premarket Approval

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 353
Devices cleared under the same product code (DXY) and FDA review panel - the closest regulatory comparables to K820356.
PULSE GENERATOR 678 B
K820657 · Siemens Elema AB · Apr 1982
IMPLANTABLE, MULTIPROGRAMMABLE
K820774 · Biotronik Sales, Inc. · Apr 1982
QUANTUM MODELS 253-09, 254-09 254-10
K820853 · Intermedics, Inc. · Apr 1982
COMMAND ULTRA I
K820231 · Cardiac Pacemakers, Inc. · Mar 1982
MEDICAL MULTILITH PULSE GENERA-1140
K813246 · Ela Medical, Inc. · Feb 1982
COMMAND P5
K813534 · Cardiac Pacemakers, Inc. · Jan 1982