Cleared Traditional

K902469 - BYRD DILATOR SHEATH SET - TEFLON

K902469 is an FDA 510(k) clearance for BYRD DILATOR SHEATH SET - TEFLON, manufactured by Medical Engineering and Development Institute. The device is a Class 2 Cardiovascular device with product code DRE cleared through the Traditional 510(k) pathway after a 80-day FDA review.

K902469 · Medical Engineering and Development Institute · Cardiovascular device
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Aug 1990
Decision
80d
Days
Class 2
Risk

K902469 is an FDA 510(k) clearance for the BYRD DILATOR SHEATH SET - TEFLON. Classified as Dilator, Vessel, For Percutaneous Catheterization (product code DRE), Class II - Special Controls.

Submitted by Medical Engineering and Development Institute (West Lafayette, US). The FDA issued a Cleared decision on August 23, 1990 after a review of 80 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1310 - 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 Medical Engineering and Development Institute devices

FDA 510(k) Submission Details - K902469

510(k) Number K902469 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 04, 1990
Decision Date August 23, 1990
Days to Decision 80 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
45d faster than avg
Panel avg: 125d · This submission: 80d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DRE Device Classification - Class 2, Special Controls

Product Code DRE Dilator, Vessel, For Percutaneous Catheterization
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.1310
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 - DRE Dilator, Vessel, For Percutaneous Catheterization

All 86
Devices cleared under the same product code (DRE) and FDA review panel - the closest regulatory comparables to K902469.
WORKSTATION FEMORAL INTRAVASCULAR RETRIEVAL (MODI)
K914555 · Med Institute, Inc. · Jan 1992
VESSEL DILATOR
K913027 · Deseret Medical, Inc. · Nov 1991
VESSEL DILATOR
K904476 · Datascope Corp. · Dec 1990
MODIFIED STERILIZATION OF INTRA-ART(TM) CORONARY
K901815 · Pioneering Technologies, Inc. · Jul 1990
SOLOSTICK (AMPLATZ DILATOR NEEDLE)
K896096 · Microvena Corp. · Apr 1990
DAIG VESSEL DILATOR
K894330 · Daig Corp. · Sep 1989