Cleared Traditional

K833061 - C-FLEX PENROSE DRAINAGE TUBE

K833061 is an FDA 510(k) clearance for C-FLEX PENROSE DRAINAGE TUBE, manufactured by Concept, Inc.. The device is a Class 2 Gastroenterology & Urology device with product code FFA cleared through the Traditional 510(k) pathway after a 59-day FDA review.

K833061 · Concept, Inc. · Gastroenterology & Urology device
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Nov 1983
Decision
59d
Days
Class 2
Risk

K833061 is an FDA 510(k) clearance for the C-FLEX PENROSE DRAINAGE TUBE. Classified as Tube, Drainage, Suprapubic (product code FFA), Class II - Special Controls.

Submitted by Concept, Inc. (Mchenry, US). The FDA issued a Cleared decision on November 7, 1983 after a review of 59 days - a notably fast clearance cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.5090 - the FDA gastroenterology and urology 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 Concept, Inc. devices

FDA 510(k) Submission Details - K833061

510(k) Number K833061 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 09, 1983
Decision Date November 07, 1983
Days to Decision 59 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
71d faster than avg
Panel avg: 130d · This submission: 59d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FFA Device Classification - Class 2, Special Controls

Product Code FFA Tube, Drainage, Suprapubic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.5090
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 Gastroenterology & Urology devices follow this clearance model.