Cleared Traditional

K823303 - QUILL CATHETER GUIDE

K823303 is the FDA 510(k) clearance for QUILL CATHETER GUIDE by Medigroup. It is a Class 2 Gastroenterology & Urology device (product code FKX) cleared through the Traditional 510(k) pathway after a 82-day FDA review.

K823303 · Medigroup · Gastroenterology & Urology device
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Jan 1983
Decision
82d
Days
Class 2
Risk

K823303 is an FDA 510(k) clearance for the QUILL CATHETER GUIDE. Classified as System, Peritoneal, Automatic Delivery (product code FKX), Class II - Special Controls.

Submitted by Medigroup (Mchenry, US). The FDA issued a Cleared decision on January 26, 1983 after a review of 82 days - a notably fast clearance cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.5630 - 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 Medigroup devices

Submission Details

510(k) Number K823303 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 05, 1982
Decision Date January 26, 1983
Days to Decision 82 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
48d faster than avg
Panel avg: 130d · This submission: 82d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code FKX System, Peritoneal, Automatic Delivery
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.5630
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.

Regulatory Peers - FKX System, Peritoneal, Automatic Delivery

All 58
Devices cleared under the same product code (FKX) and FDA review panel - the closest regulatory comparables to K823303.
ABBOTT PATIENT ASSIST DEVICE
K830766 · Abbott Laboratories · Mar 1983
AMP 80/2 OUTFLOW MONITOR MODIFICATION
K823827 · American Medical Products, Inc. · Mar 1983
BETA-CAP D ADAPTER
K830208 · Quinton, Inc. · Mar 1983
IMPRA PERITONEAL CATHETER
K823857 · Impra, Inc. · Jan 1983
STERILE, DISPOS. SPIKE PROTECTOR-5C4138
K823777 · Travenol Laboratories, S.A. · Jan 1983
INPERSOL PERITONEAL DIALSIS CYCLER SET
K823217 · Abbott Laboratories · Nov 1982