Cleared Traditional

K810492 - TYPE YR ENDOCARDIAL LEAD

K810492 is an FDA 510(k) clearance for TYPE YR ENDOCARDIAL LEAD, manufactured by Biotronik Sales, Inc.. The device is a Class 3 Cardiovascular device with product code DTB cleared through the Traditional 510(k) pathway after a 24-day FDA review.

K810492 · Biotronik Sales, Inc. · Cardiovascular device
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Mar 1981
Decision
24d
Days
Class 3
Risk

K810492 is an FDA 510(k) clearance for the TYPE YR ENDOCARDIAL LEAD. Classified as Permanent Pacemaker Electrode (product code DTB), Class III - Premarket Approval.

Submitted by Biotronik Sales, Inc. (Mchenry, US). The FDA issued a Cleared decision on March 20, 1981 after a review of 24 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 Biotronik Sales, Inc. devices

FDA 510(k) Submission Details - K810492

510(k) Number K810492 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 24, 1981
Decision Date March 20, 1981
Days to Decision 24 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
101d faster than avg
Panel avg: 125d · This submission: 24d
Pathway characteristics
Predicate-based equivalence.

DTB Device Classification - Class 3, Premarket Approval

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 396
Devices cleared under the same product code (DTB) and FDA review panel - the closest regulatory comparables to K810492.
CORDIS ENCOR PEWENOUS VENTRICULAR BIPOL
K811539 · Cordis Corp. · Jul 1981
INTERMEDICS POLY FLEX ENDOCARDIAL PACING
K811106 · Intermedics, Inc. · May 1981
TYPE YC ENDOCARDIAL LEAD
K810491 · Biotronik Sales, Inc. · Mar 1981
TYPE N ENDOCARDIAL LEAD
K810493 · Biotronik Sales, Inc. · Mar 1981
TEMPORARY MYOCARDIAL PACING LEAD#6400
K810333 · Medtronic Vascular · Mar 1981
CORDIS PERVENOUS ATRIAL LEAD
K810432 · Cordis Corp. · Mar 1981