Cleared Traditional

K771482 - RINSE BLOCK CONNECTOR

K771482 is the FDA 510(k) clearance for RINSE BLOCK CONNECTOR by Quinton, Inc.. It is a Class 2 Gastroenterology & Urology device (product code KDJ) cleared through the Traditional 510(k) pathway after a 152-day FDA review.

K771482 · Quinton, Inc. · Gastroenterology & Urology device
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Jan 1978
Decision
152d
Days
Class 2
Risk

K771482 is an FDA 510(k) clearance for the RINSE BLOCK CONNECTOR. Classified as Set, Administration, For Peritoneal Dialysis, Disposable (product code KDJ), Class II - Special Controls.

Submitted by Quinton, Inc. (Mchenry, US). The FDA issued a Cleared decision on January 3, 1978 after a review of 152 days - an extended review 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Gastroenterology & Urology review framework, consistent with the majority of Class II 510(k) submissions.

View all Quinton, Inc. devices

Submission Details

510(k) Number K771482 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 04, 1977
Decision Date January 03, 1978
Days to Decision 152 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
22d slower than avg
Panel avg: 130d · This submission: 152d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code KDJ Set, Administration, For Peritoneal Dialysis, Disposable
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 - KDJ Set, Administration, For Peritoneal Dialysis, Disposable

All 87
Devices cleared under the same product code (KDJ) and FDA review panel - the closest regulatory comparables to K771482.
SET, ADMINISTRATION, MANUAL, DIALYSIS
K780957 · American Medical Products, Inc. · Jul 1978
FILTER, PERITONEAL DIALY. ADMIN. SET
K772236 · Millipore Corp. · Jan 1978
PERITONEAL DIALYSIS ADMIN. SET
K780082 · Physio-Control Corp. · Jan 1978
PERITONEAL CYCLER & MANIFOLD SET
K772136 · Physio-Control Corp. · Dec 1977