Cleared Traditional

K781252 - GENERATOR

K781252 is the FDA 510(k) clearance for GENERATOR by Medtronic Vascular. It is a Class 3 Cardiovascular device (product code DXY) cleared through the Traditional 510(k) pathway after a 74-day FDA review.

K781252 · Medtronic Vascular · Cardiovascular device
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Oct 1978
Decision
74d
Days
Class 3
Risk

K781252 is an FDA 510(k) clearance for the GENERATOR, PULSE, MODEL 5997. Classified as Implantable Pacemaker Pulse-generator (product code DXY), Class III - Premarket Approval.

Submitted by Medtronic Vascular (Walker, US). The FDA issued a Cleared decision on October 3, 1978 after a review of 74 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 Medtronic Vascular devices

Submission Details

510(k) Number K781252 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 21, 1978
Decision Date October 03, 1978
Days to Decision 74 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
51d faster than avg
Panel avg: 125d · This submission: 74d
Pathway characteristics
Predicate-based equivalence.

Device Classification

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 338
Devices cleared under the same product code (DXY) and FDA review panel - the closest regulatory comparables to K781252.
PACEMAKER, MODEL 229-01
K781738 · Intermedics, Inc. · Dec 1978
GENERATOR, PULSE, SORIN MODEL DL-1
K780897 · Bentley Laboratories, Inc. · Dec 1978
GENERATORS, PULSE, MODELS 5988/5989
K781208 · Medtronic Vascular · Oct 1978
PACEMAKER, MODEL 225 & 227
K772226 · Intermedics, Inc. · Sep 1978
GENERATOR, PULSE, MODEL 160B
K780940 · Telectronics, Inc. · Sep 1978
GENERATORS: UDL-201B, BDL-201B, MDL-201B
K781424 · Pacesetter Systems · Sep 1978