Cleared Traditional

K831376 - CDS 2001 ARTIFICIAL KIDNEY

K831376 is the FDA 510(k) clearance for CDS 2001 ARTIFICIAL KIDNEY by Elmar Medical Systems, Ltd.. It is a Class 2 Gastroenterology & Urology device (product code KOC) cleared through the Traditional 510(k) pathway after a 37-day FDA review.

K831376 · Elmar Medical Systems, Ltd. · Gastroenterology & Urology device
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Jun 1983
Decision
37d
Days
Class 2
Risk

K831376 is an FDA 510(k) clearance for the CDS 2001 ARTIFICIAL KIDNEY. Classified as Accessories, Blood Circuit, Hemodialysis (product code KOC), Class II - Special Controls.

Submitted by Elmar Medical Systems, Ltd. (Mchenry, US). The FDA issued a Cleared decision on June 3, 1983 after a review of 37 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 Elmar Medical Systems, Ltd. devices

Submission Details

510(k) Number K831376 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 27, 1983
Decision Date June 03, 1983
Days to Decision 37 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
93d faster than avg
Panel avg: 130d · This submission: 37d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

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 122
Devices cleared under the same product code (KOC) and FDA review panel - the closest regulatory comparables to K831376.
SINGLE PATIENT SYS. II MODEL DM-450
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K832252 · Terumo Medical Corp. · Aug 1983
GF-180-L HOLLOW FIBER HEMODIALYSIS
K831606 · Gambro, Inc. · Jun 1983
CLIRANS TAF 120 HOLLOW FIBER DIALYZ. &
K831482 · Terumo Medical Corp. · Jun 1983
EXTRASENSR ULTRAFILTRATION MONITOR
K831433 · Extracorporeal Medical Specialities, Inc. · Jun 1983
LUNDIA 10-3-L PARALLEL FLOW DIALYZER
K831338 · Gambro, Inc. · May 1983