Cleared Traditional

K926109 - FLUID DRAINAGE TRAY

K926109 is an FDA 510(k) clearance for FLUID DRAINAGE TRAY, manufactured by Symbiosis Corp.. The device is a Class 1 General & Plastic Surgery device with product code GBX cleared through the Traditional 510(k) pathway after a 186-day FDA review.

K926109 · Symbiosis Corp. · General & Plastic Surgery device
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Jun 1993
Decision
186d
Days
Class 1
Risk

K926109 is an FDA 510(k) clearance for the FLUID DRAINAGE TRAY. Classified as Catheter, Irrigation (product code GBX), Class I - General Controls.

Submitted by Symbiosis Corp. (Miami, US). The FDA issued a Cleared decision on June 7, 1993 after a review of 186 days - an extended review 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General & Plastic Surgery review framework, consistent with the majority of Class II 510(k) submissions.

View all Symbiosis Corp. devices

FDA 510(k) Submission Details - K926109

510(k) Number K926109 FDA.gov
FDA Decision Cleared Substantially Equivalent - De Novo Granted (SEKD)
Date Received December 03, 1992
Decision Date June 07, 1993
Days to Decision 186 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
71d slower than avg
Panel avg: 115d · This submission: 186d
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 33
Devices cleared under the same product code (GBX) and FDA review panel - the closest regulatory comparables to K926109.
SIL-SLIP ROUND WOUND DRAIN (COATED)/BLUE STRIPE
K926495 · Sil-Med Corp. · Feb 1994
ERCP CATHETER, HYDROPHILIC COATED
K932205 · Wilson-Cook Medical, Inc. · Jan 1994
URESIL ABSCESS DRIANAGE AND IRRIGATION SET
K925117 · Uresil Corp. · Aug 1993
KENDALL UNIVERSAL EXTENSION SET
K930551 · Kendall Healthcare Products Co. Div.Of Tyco Health · May 1993
VANSONNENBERG CHEST DRAINAGE CATHETER ALL PURPOSE
K925176 · Boston Scientific Corp · Apr 1993
KENDALL WOUND DRAINAGE SYSTEMS-TROCARS
K925805 · Kendall Healthcare Products Co. Div.Of Tyco Health · Feb 1993