Cleared Traditional

K823715 - SINGLE ACCESS DEVICE (SSAD)

K823715 is an FDA 510(k) clearance for SINGLE ACCESS DEVICE (SSAD), manufactured by Samaritan Hospital. The device is a Class 2 Gastroenterology & Urology device with product code KOC cleared through the Traditional 510(k) pathway after a 59-day FDA review.

K823715 · Samaritan Hospital · Gastroenterology & Urology device
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Feb 1983
Decision
59d
Days
Class 2
Risk

K823715 is an FDA 510(k) clearance for the SINGLE ACCESS DEVICE (SSAD). Classified as Accessories, Blood Circuit, Hemodialysis (product code KOC), Class II - Special Controls.

Submitted by Samaritan Hospital (Walker, US). The FDA issued a Cleared decision on February 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 876.5820 - 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 Samaritan Hospital devices

FDA 510(k) Submission Details - K823715

510(k) Number K823715 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 10, 1982
Decision Date February 07, 1983
Days to Decision 59 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
72d faster than avg
Panel avg: 131d · This submission: 59d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KOC Device Classification - Class 2, Special Controls

Product Code KOC Accessories, Blood Circuit, Hemodialysis
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.5820
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 - KOC Accessories, Blood Circuit, Hemodialysis

All 142
Devices cleared under the same product code (KOC) and FDA review panel - the closest regulatory comparables to K823715.
KF-101-07 DIALYZER
K822337 · Extracorporeal Medical Specialities, Inc. · Feb 1983
KF-101-10 DIALYZER
K822338 · Extracorporeal Medical Specialities, Inc. · Feb 1983
KF-101-13 DIALYZER
K822339 · Extracorporeal Medical Specialities, Inc. · Feb 1983
MEDISYSTEMS FISTULA NEEDLES
K823068 · Medisystems Corp. · Jan 1983
KF-E SERIES HOLLOW FIBER DIALYZER
K823069 · Medisystems Corp. · Jan 1983
A.V. FISTULA CANNULATION SETS
K830021 · Travenol Laboratories, S.A. · Jan 1983