Cleared Traditional

LIFELINE TLE J-SHAPED ATRIAL ENDOCARDIAL (K792301) - FDA 510(k) Clearance

Class III device cleared through the 510(k) pathway via substantial equivalence to a legally marketed predicate.

K792301 · Intermedics, Inc. · Cardiovascular device
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Jun 1980
Decision
202d
Days
Class 3
Risk

K792301 is an FDA 510(k) clearance for the LIFELINE TLE J-SHAPED ATRIAL ENDOCARDIAL. Classified as Permanent Pacemaker Electrode (product code DTB), Class III - Premarket Approval.

Submitted by Intermedics, Inc. (Mchenry, US). The FDA issued a Cleared decision on June 4, 1980 after a review of 202 days - an extended review 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 Intermedics, Inc. devices

Submission Details

510(k) Number K792301 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 15, 1979
Decision Date June 04, 1980
Days to Decision 202 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
77d slower than avg
Panel avg: 125d · This submission: 202d
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 221
Devices cleared under the same product code (DTB) and FDA review panel - the closest regulatory comparables to K792301.
IMPLANTABLE ENDOCARDIAL POROUS TIP ELEC.
K801792 · Telectronics, Inc. · Oct 1980
MEDTRONIC MODEL 69575
K800944 · Medtronic Vascular · Sep 1980
LIFELINE TLE (TRAEBECULAR LODGING ELEC
K792300 · Intermedics, Inc. · Jun 1980
RESTERILIZATION OF IMPLANTABLE ELECTRODE
K800891 · Telectronics, Inc. · May 1980
LIFELINE TLE ENDOCARDIAL PACING LEAD,
K792604 · Intermedics, Inc. · Dec 1979
IMPLANTABLE END. MUSH. TIP LEADS030-224
K792321 · Telectronics, Inc. · Dec 1979