Cleared Traditional

K881073 - SHILEY FEMORAL CANNULAE INTRODUCER KIT

K881073 is an FDA 510(k) clearance for SHILEY FEMORAL CANNULAE INTRODUCER KIT, manufactured by Shiley, Inc.. The device is a Class 2 Cardiovascular device with product code DRE cleared through the Traditional 510(k) pathway after a 87-day FDA review.

K881073 · Shiley, Inc. · Cardiovascular device
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Jun 1988
Decision
87d
Days
Class 2
Risk

K881073 is an FDA 510(k) clearance for the SHILEY FEMORAL CANNULAE INTRODUCER KIT. Classified as Dilator, Vessel, For Percutaneous Catheterization (product code DRE), Class II - Special Controls.

Submitted by Shiley, Inc. (Irvine, US). The FDA issued a Cleared decision on June 9, 1988 after a review of 87 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 Shiley, Inc. devices

FDA 510(k) Submission Details - K881073

510(k) Number K881073 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 14, 1988
Decision Date June 09, 1988
Days to Decision 87 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
38d faster than avg
Panel avg: 125d · This submission: 87d
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 50
Devices cleared under the same product code (DRE) and FDA review panel - the closest regulatory comparables to K881073.
WORKSTATION FEMORAL INTRAVASCULAR RETRIEVAL (MODI)
K914555 · Med Institute, Inc. · Jan 1992
VESSEL DILATOR
K904476 · Datascope Corp. · Dec 1990
DAIG VESSEL DILATOR
K894330 · Daig Corp. · Sep 1989
10 AND 12 FRENCH VESSEL DILATORS
K874738 · Impra, Inc. · May 1988
URESIL CAROTID ARTERY SIZERS
K871148 · Uresil Corp. · Apr 1987
MODIFICATION OF TISSUE DILATOR
K862288 · Quinton, Inc. · Aug 1986