Cleared Traditional

K792252 - DMS 3000

K792252 is the FDA 510(k) clearance for DMS 3000 by Renal Care Corp.. It is a Class 2 Gastroenterology & Urology device (product code FKQ) cleared through the Traditional 510(k) pathway after a 125-day FDA review.

K792252 · Renal Care Corp. · Gastroenterology & Urology device
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Mar 1980
Decision
125d
Days
Class 2
Risk

K792252 is an FDA 510(k) clearance for the DMS 3000. Classified as System, Dialysate Delivery, Central Multiple Patient (product code FKQ), Class II - Special Controls.

Submitted by Renal Care Corp. (Mchenry, US). The FDA issued a Cleared decision on March 12, 1980 after a review of 125 days - within the typical 510(k) review window.

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: 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 Renal Care Corp. devices

Submission Details

510(k) Number K792252 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 08, 1979
Decision Date March 12, 1980
Days to Decision 125 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
5d faster than avg
Panel avg: 130d · This submission: 125d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code FKQ System, Dialysate Delivery, Central Multiple Patient
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 - FKQ System, Dialysate Delivery, Central Multiple Patient

All 32
Devices cleared under the same product code (FKQ) and FDA review panel - the closest regulatory comparables to K792252.
MODEL DM-333 DIALYSIS CONTROL STATION
K811444 · Extracorporeal Medical Specialities, Inc. · Jun 1981
ALTERNATE STERILIZ. FOR CELLULOSE ACET
K810315 · Cordis Corp. · Mar 1981
MOD. DM-356 IPS INTERFACE MODULE
K800771 · Extracorporeal Medical Specialities, Inc. · May 1980
PATIENT AID, MODEL DM-351
K781176 · Extracorporeal Medical Specialities, Inc. · Sep 1978
DIALYZING FLUIDE DELIVERY SYSTEM
K780081 · Travenol Laboratories, S.A. · Mar 1978
PRESSURE MODULE 5M1247
K771375 · Travenol Laboratories, S.A. · Sep 1977