Cleared Traditional

K874632 - BENT NECK CURLCATH PERITONEAL DIALYSIS KIT

K874632 is the FDA 510(k) clearance for BENT NECK CURLCATH PERITONEAL DIALYSIS KIT by Quinton, Inc.. It is a Class 2 Gastroenterology & Urology device (product code FKX) cleared through the Traditional 510(k) pathway after a 50-day FDA review.

K874632 · Quinton, Inc. · Gastroenterology & Urology device
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Dec 1987
Decision
50d
Days
Class 2
Risk

K874632 is an FDA 510(k) clearance for the BENT NECK CURLCATH PERITONEAL DIALYSIS KIT. Classified as System, Peritoneal, Automatic Delivery (product code FKX), Class II - Special Controls.

Submitted by Quinton, Inc. (Seattle, US). The FDA issued a Cleared decision on December 29, 1987 after a review of 50 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 Quinton, Inc. devices

Submission Details

510(k) Number K874632 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 09, 1987
Decision Date December 29, 1987
Days to Decision 50 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
80d faster than avg
Panel avg: 130d · This submission: 50d
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 57
Devices cleared under the same product code (FKX) and FDA review panel - the closest regulatory comparables to K874632.
NMC CYCLER MACHINE
K905809 · National Medical Care, Medical Products Div., Inc. · Feb 1992
ABBOTT INPERSOL CYCLER 1000
K895336 · Abbott Laboratories · Nov 1989
PERITONEAL CATHETER STABILIZATION DEVICE 5C4381
K884554 · Baxter Healthcare Corp · Jan 1989
UPGRADED AUTO PERITONEAL DIALYSIS CYCLER SYSTEM
K872652 · Travenol Laboratories, S.A. · Sep 1987
ABBOTT INPERSOL CYCLER 1000
K845042 · Abbott Laboratories · Mar 1985
ROPE SYSTEM REVERSE OSMOSIS PERITONEAL SYSTEM
K844630 · Organon Teknika Corp. · Mar 1985