Cleared Traditional

K935998 - ENTERPRISE

K935998 is an FDA 510(k) clearance for ENTERPRISE, manufactured by Camp Intl., Inc.. The device is a Class 2 Cardiovascular device with product code DQX cleared through the Traditional 510(k) pathway after a 702-day FDA review.

K935998 · Camp Intl., Inc. · Cardiovascular device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Nov 1995
Decision
702d
Days
Class 2
Risk

K935998 is an FDA 510(k) clearance for the ENTERPRISE. Classified as Wire, Guide, Catheter (product code DQX), Class II - Special Controls.

Submitted by Camp Intl., Inc. (Grand Rapids, US). The FDA issued a Cleared decision on November 17, 1995 after a review of 702 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1330 - 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. Elevated predicate reliance profile. The extended review timeline suggests the FDA required additional documentation before confirming substantial equivalence - a pattern common in complex or first-of-kind Cardiovascular submissions.

View all Camp Intl., Inc. devices

FDA 510(k) Submission Details - K935998

510(k) Number K935998 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 15, 1993
Decision Date November 17, 1995
Days to Decision 702 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
577d slower than avg
Panel avg: 125d · This submission: 702d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DQX Device Classification - Class 2, Special Controls

Product Code DQX Wire, Guide, Catheter
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.1330
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 - DQX Wire, Guide, Catheter

All 697
Devices cleared under the same product code (DQX) and FDA review panel - the closest regulatory comparables to K935998.
RADIFOCUS GLIDEWIRE GT WITH GOLD COIL,GLIDEWIRE GOLD
K955801 · Terumo Medical Corp. · Feb 1996
GUIDE WIRE FOR THE USE WITH DATASCOPE PERCOR STAT-DL IABS
K943896 · Datascope Corp. · Dec 1995
THE NINER NITINOL GUIDEWIRE
K952860 · Microvena Corp. · Dec 1995
CORDIS WIZDOM STEERABLE GUIDEWIRE
K953760 · Cordis Corp. · Nov 1995
CARDIOMETRICS ACCUTRAC INTRAVASCULAR GUIDE WIRE (MODIFICATION)
K954913 · Cardio Metrics, Inc. · Nov 1995
RADIFOCUS GLIDEWIRE FOR CORONARY USE WITH PLATINUM (OR GOLD) COIL
K953533 · Terumo Medical Corp. · Oct 1995