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.
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