Cleared Traditional

K894040 - IMPLANTABLE PACING LEADS W/IS-1 CONN.

K894040 is the FDA 510(k) clearance for IMPLANTABLE PACING LEADS W/IS-1 CONN. by Medtronic Vascular. It is a Class 3 Cardiovascular device (product code DTB) cleared through the Traditional 510(k) pathway after a 38-day FDA review.

K894040 · Medtronic Vascular · Cardiovascular device
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Jul 1989
Decision
38d
Days
Class 3
Risk

K894040 is an FDA 510(k) clearance for the IMPLANTABLE PACING LEADS W/IS-1 CONN., UNIPOLAR. Classified as Permanent Pacemaker Electrode (product code DTB), Class III - Premarket Approval.

Submitted by Medtronic Vascular (Minneapolis, US). The FDA issued a Cleared decision on July 14, 1989 after a review of 38 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.3680 - 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 K894040 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 06, 1989
Decision Date July 14, 1989
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.

Device Classification

Product Code DTB Permanent Pacemaker Electrode
Device Class Class 3 - Premarket Approval
CFR Regulation 21 CFR 870.3680
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 - DTB Permanent Pacemaker Electrode

All 364
Devices cleared under the same product code (DTB) and FDA review panel - the closest regulatory comparables to K894040.
MYOPORE(TM) UNIPOLAR MODELS 1117 & 1118 PACE LEADS
K896443 · Possis Medical, Inc. · Dec 1989
MYOPORE(TM) UNIPOLAR SUTURELESS MYOCARDIAL LEADS
K885175 · Possis Medical, Inc. · Jul 1989
MODELS 1113 AND 1114 PACEMAKER LEADS
K893763 · Possis Medical, Inc. · Jul 1989
PACEMAKER LEAD ADAPTER
K890018 · Ela Medical, Inc. · Jun 1989
CARDIOVASCULAR PERMANENT PACEMAKER ELECTRODE
K891905 · Pacesetter Systems · Jun 1989
MEDTRONIC MODEL 5866-45 SIZING SLEEVE
K890644 · Medtronic Vascular · May 1989