Cleared Traditional

K062302 - MILLICORE AB DIGIVENT CHEST DRAINAGE SYSTEM

K062302 is an FDA 510(k) clearance for MILLICORE AB DIGIVENT CHEST DRAINAGE SYSTEM, manufactured by Millicore AB. The device is a Class 2 General Hospital device with product code KDQ cleared through the Traditional 510(k) pathway after a 59-day FDA review.

K062302 · Millicore AB · General Hospital
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Oct 2006
Decision
59d
Days
Class 2
Risk

K062302 is an FDA 510(k) clearance for the MILLICORE AB DIGIVENT CHEST DRAINAGE SYSTEM. Classified as Bottle, Collection, Vacuum (product code KDQ), Class II - Special Controls.

Submitted by Millicore AB (North Attleboro, US). The FDA issued a Cleared decision on October 6, 2006 after a review of 59 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6740 - the FDA general hospital device 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 Millicore AB devices

FDA 510(k) Submission Details - K062302

510(k) Number K062302 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 08, 2006
Decision Date October 06, 2006
Days to Decision 59 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
70d faster than avg
Panel avg: 129d · This submission: 59d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KDQ Device Classification - Class 2, Special Controls

Product Code KDQ Bottle, Collection, Vacuum
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.6740
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 General Hospital devices follow this clearance model.

Regulatory Peers - KDQ Bottle, Collection, Vacuum

All 36
Devices cleared under the same product code (KDQ) and FDA review panel - the closest regulatory comparables to K062302.
EXPRESS CHEST DRAIN
K081718 · Atrium Medical Corp. · Jul 2008
OCEAN CHEST DRAIN
K043582 · Atrium Medical Corp. · Jan 2005
ATRIUM MEDICAL CORPORATION EXPRESS CHEST DRAIN
K984496 · Atrium Medical Corp. · May 1999
PLEUR-EVAC SAHARA ADULT/PEDIATRIC CHEST DRAINAGE SYSTEM MODEL S-1100, S-1200, 2-2100, AND S-2200 WITH MODEL S-100 AUTOTR
K962856 · Deknatel, Inc. · Aug 1996
ROCKET PLEURASEAL II CHEST DRAINAGE SYSTEM
K961287 · Rocket Medical Plc · Jul 1996
MUCUS SPECIMEN TRAP
K962168 · Sage Products, Inc. · Jul 1996