Cleared Traditional

K802864 - SIEMENS-ELEMA PULSE GENERATOR 678

K802864 is an FDA 510(k) clearance for SIEMENS-ELEMA PULSE GENERATOR 678, manufactured by Siemens Elema AB. The device is a Class 3 Cardiovascular device with product code DXY cleared through the Traditional 510(k) pathway after a 85-day FDA review.

K802864 · Siemens Elema AB · Cardiovascular device
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Feb 1981
Decision
85d
Days
Class 3
Risk

K802864 is an FDA 510(k) clearance for the SIEMENS-ELEMA PULSE GENERATOR 678. Classified as Implantable Pacemaker Pulse-generator (product code DXY), Class III - Premarket Approval.

Submitted by Siemens Elema AB (Mchenry, US). The FDA issued a Cleared decision on February 5, 1981 after a review of 85 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.3610 - 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 Siemens Elema AB devices

FDA 510(k) Submission Details - K802864

510(k) Number K802864 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 12, 1980
Decision Date February 05, 1981
Days to Decision 85 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
40d faster than avg
Panel avg: 125d · This submission: 85d
Pathway characteristics
Predicate-based equivalence.

DXY Device Classification - Class 3, Premarket Approval

Product Code DXY Implantable Pacemaker Pulse-generator
Device Class Class 3 - Premarket Approval
CFR Regulation 21 CFR 870.3610
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 - DXY Implantable Pacemaker Pulse-generator

All 339
Devices cleared under the same product code (DXY) and FDA review panel - the closest regulatory comparables to K802864.
THINLITH II PULSE GNEERATOR MODEL 227-05
K810386 · Intermedics, Inc. · Mar 1981
STERILE PACKAGING
K810410 · Telectronics, Inc. · Mar 1981
MULTI-PROGRAMMABLE PACEMAKER & PROGRMR.
K801584 · Medtronic Vascular · Feb 1981
SIEMENS-ELEMA MYOCARDIAL LEAD
K810036 · Siemens Elema AB · Jan 1981
IMPL. PROGRAMMABLE BIPOLAR CARD.GEN.#274
K803197 · Telectronics, Inc. · Jan 1981
CYBERLITH PROGRAMMER
K801338 · Intermedics, Inc. · Jan 1981