Cleared Traditional

K893633 - MODEL 5330 EXTERNAL A-V SEQUENTIAL DEMAND PULSE

K893633 is an FDA 510(k) clearance for MODEL 5330 EXTERNAL A-V SEQUENTIAL DEMA..., manufactured by Medtronic Vascular. The device is a Class 2 Cardiovascular device with product code DTE cleared through the Traditional 510(k) pathway after a 40-day FDA review.

K893633 · Medtronic Vascular · Cardiovascular device
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Jun 1989
Decision
40d
Days
Class 2
Risk

K893633 is an FDA 510(k) clearance for the MODEL 5330 EXTERNAL A-V SEQUENTIAL DEMAND PULSE. Classified as Pulse-generator, Pacemaker, External (product code DTE), Class II - Special Controls.

Submitted by Medtronic Vascular (Minneapolis, US). The FDA issued a Cleared decision on June 20, 1989 after a review of 40 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.3600 - 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Medtronic Vascular devices

FDA 510(k) Submission Details - K893633

510(k) Number K893633 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 11, 1989
Decision Date June 20, 1989
Days to Decision 40 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
85d faster than avg
Panel avg: 125d · This submission: 40d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DTE Device Classification - Class 2, Special Controls

Product Code DTE Pulse-generator, Pacemaker, External
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.3600
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Cardiovascular devices follow this clearance model.

Regulatory Peers - DTE Pulse-generator, Pacemaker, External

All 54
Devices cleared under the same product code (DTE) and FDA review panel - the closest regulatory comparables to K893633.
MODIFIED MODEL 5330 AV DEMAND PULSE GENERATOR
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