Cleared Traditional

K791722 - DISPOSABLE PERITONEAL DIALYSIS EXTENSION

K791722 is an FDA 510(k) clearance for DISPOSABLE PERITONEAL DIALYSIS EXTENSION, manufactured by American Medical Products, Inc.. The device is a Class 2 Gastroenterology & Urology device with product code KDJ cleared through the Traditional 510(k) pathway after a 78-day FDA review.

K791722 · American Medical Products, Inc. · Gastroenterology & Urology device
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Nov 1979
Decision
78d
Days
Class 2
Risk

K791722 is an FDA 510(k) clearance for the DISPOSABLE PERITONEAL DIALYSIS EXTENSION. Classified as Set, Administration, For Peritoneal Dialysis, Disposable (product code KDJ), Class II - Special Controls.

Submitted by American Medical Products, Inc. (Mchenry, US). The FDA issued a Cleared decision on November 16, 1979 after a review of 78 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 American Medical Products, Inc. devices

FDA 510(k) Submission Details - K791722

510(k) Number K791722 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 30, 1979
Decision Date November 16, 1979
Days to Decision 78 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
53d faster than avg
Panel avg: 131d · This submission: 78d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KDJ Device Classification - Class 2, Special Controls

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 100
Devices cleared under the same product code (KDJ) and FDA review panel - the closest regulatory comparables to K791722.
PERITONEAL DIALYSIS CYCLER SET W/PUMP
K801220 · American Medical Products, Inc. · Aug 1980
CONTINUOUS AMBULATORY DIALYSIS (CAPD)
K791512 · Norton Performance Plastics Corp. · Feb 1980
CAPD TRANSFER SET JC9044
K792651 · Travenol Laboratories, S.A. · Feb 1980
CYCLER SETS MOD. #5C4143, 5C4144, 5C4145
K791899 · Travenol Laboratories, S.A. · Nov 1979
SET, ADMINISTRATION, MANUAL, DIALYSIS
K780957 · American Medical Products, Inc. · Jul 1978
FILTER, PERITONEAL DIALY. ADMIN. SET
K772236 · Millipore Corp. · Jan 1978