Cleared Traditional

K052286 - DEUTSCH ANTI-BLOCKAGE WOUND DRAIN

K052286 is an FDA 510(k) clearance for DEUTSCH ANTI-BLOCKAGE WOUND DRAIN, manufactured by The Catheter Exchange, Inc.. The device is a Class 1 General & Plastic Surgery device with product code GBX cleared through the Traditional 510(k) pathway after a 60-day FDA review.

K052286 · The Catheter Exchange, Inc. · General & Plastic Surgery device
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Oct 2005
Decision
60d
Days
Class 1
Risk

K052286 is an FDA 510(k) clearance for the DEUTSCH ANTI-BLOCKAGE WOUND DRAIN. Classified as Catheter, Irrigation (product code GBX), Class I - General Controls.

Submitted by The Catheter Exchange, Inc. (Encino, US). The FDA issued a Cleared decision on October 21, 2005 after a review of 60 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4200 - the FDA general and plastic surgery 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 The Catheter Exchange, Inc. devices

FDA 510(k) Submission Details - K052286

510(k) Number K052286 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 22, 2005
Decision Date October 21, 2005
Days to Decision 60 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
55d faster than avg
Panel avg: 115d · This submission: 60d
Pathway characteristics
Predicate-based equivalence.

GBX Device Classification - Class 1, General Controls

Product Code GBX Catheter, Irrigation
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.4200
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - GBX Catheter, Irrigation

All 45
Devices cleared under the same product code (GBX) and FDA review panel - the closest regulatory comparables to K052286.
MISONIX IRRIGATION SYSTEM MOEDL BC20P
K013417 · Misonix, Inc. · Jan 2002
LYSONIX IRRIGATION SYSTEM
K974233 · Lysonix, Inc. · Feb 1998
JACKSON-PRATT HEMADUCT WOUND DRAIN, JACKSON-PRATT GOLD HEMADUCT WOUND DRAIN
K973703 · Allegiance Healthcare Corp. · Dec 1997
ULTRACELL SUCTION SPONGE
K972635 · Ultracell Medical Technologies, Inc. · Oct 1997
FLAT CLOSED WOUND DRAIN WITH TROCAR
K965146 · Axiom Medical, Inc. · Mar 1997
SAPPHIRE LINE FLAT DRAIN/KIT WITH SPI-ARGENT II W/OR W/OUT TROCAR
K961295 · Sil-Med Corp. · Jun 1996