Cleared Traditional

K843837 - MEDTRONIC 5984-5984LP-5985

K843837 is the FDA 510(k) clearance for MEDTRONIC 5984-5984LP-5985 by Medtronic Vascular. It is a Class 3 Cardiovascular device (product code DXY) cleared through the Traditional 510(k) pathway after a 16-day FDA review.

K843837 · Medtronic Vascular · Cardiovascular device
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Oct 1984
Decision
16d
Days
Class 3
Risk

K843837 is an FDA 510(k) clearance for the MEDTRONIC 5984-5984LP-5985. Classified as Implantable Pacemaker Pulse-generator (product code DXY), Class III - Premarket Approval.

Submitted by Medtronic Vascular (Minneapolis, US). The FDA issued a Cleared decision on October 17, 1984 after a review of 16 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 Medtronic Vascular devices

Submission Details

510(k) Number K843837 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 01, 1984
Decision Date October 17, 1984
Days to Decision 16 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
109d faster than avg
Panel avg: 125d · This submission: 16d
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 338
Devices cleared under the same product code (DXY) and FDA review panel - the closest regulatory comparables to K843837.
MULTILITH 2 PULSE GENERATOR 1141 & 2141
K842220 · Ela Medical, Inc. · Nov 1984
IMPLANTABLE PROGRAMMABLE PULSE GENERAT
K842473 · Telectronics, Inc. · Oct 1984
ASTRA 2, ASTRA 3, 4 & 6
K842394 · Cardiac Pacemakers, Inc. · Oct 1984
MEDTRONIC 8437/8438
K843089 · Medtronic Vascular · Aug 1984
NEOS LP
K841633 · Biotronik Sales, Inc. · Aug 1984
LEPTOS
K841635 · Biotronik Sales, Inc. · Aug 1984