Cleared Traditional

K802413 - IMPLANT. ENDOCARDIAL DISH TIP ELECT. LDS

K802413 is an FDA 510(k) clearance for IMPLANT. ENDOCARDIAL DISH TIP ELECT. LDS, manufactured by Telectronics, Inc.. The device is a Class 3 Cardiovascular device with product code DTB cleared through the Traditional 510(k) pathway after a 88-day FDA review.

K802413 · Telectronics, Inc. · Cardiovascular device
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Jan 1981
Decision
88d
Days
Class 3
Risk

K802413 is an FDA 510(k) clearance for the IMPLANT. ENDOCARDIAL DISH TIP ELECT. LDS. Classified as Permanent Pacemaker Electrode (product code DTB), Class III - Premarket Approval.

Submitted by Telectronics, Inc. (Walker, US). The FDA issued a Cleared decision on January 2, 1981 after a review of 88 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 Telectronics, Inc. devices

FDA 510(k) Submission Details - K802413

510(k) Number K802413 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 06, 1980
Decision Date January 02, 1981
Days to Decision 88 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
37d faster than avg
Panel avg: 125d · This submission: 88d
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 387
Devices cleared under the same product code (DTB) and FDA review panel - the closest regulatory comparables to K802413.
PERM. ENDOCARDIAL UNIPOLAR TINED/WEDGE
K802552 · Daig Corp. · Jan 1981
PERM. ENDOCARDIAL UNIPOLAR WEDGE URETHAN
K802553 · Daig Corp. · Jan 1981
ENDOCARDIAL LEADS 414S & 515S
K802816 · Siemens Elema AB · Jan 1981
UNIPOLAR ENDOCARDIAL LASER DRILLED ELEC
K802968 · Telectronics, Inc. · Dec 1980
SIEMENS-ELEMA ENDOCARDIAL LEAD 402S
K803042 · Siemens Elema AB · Dec 1980
INTERMEDICS' LIFELINE TLE ENDOCARDIAL
K801172 · Intermedics, Inc. · Dec 1980