Cleared Traditional

K900018 - HOLLOW FIBER DIALYZER, BIO CARE PS 130

K900018 is an FDA 510(k) clearance for HOLLOW FIBER DIALYZER, manufactured by National Medical Care, Medical Products Div., Inc.. The device is a Class 2 Gastroenterology & Urology device with product code KDI cleared through the Traditional 510(k) pathway after a 206-day FDA review.

K900018 · National Medical Care, Medical Products Div., Inc. · Gastroenterology & Urology device
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Jul 1990
Decision
206d
Days
Class 2
Risk

K900018 is an FDA 510(k) clearance for the HOLLOW FIBER DIALYZER, BIO CARE PS 130. Classified as Dialyzer, High Permeability With Or Without Sealed Dialysate System (product code KDI), Class II - Special Controls.

Submitted by National Medical Care, Medical Products Div., Inc. (Rockleigh, US). The FDA issued a Cleared decision on July 27, 1990 after a review of 206 days - an extended review cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.5860 - 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 National Medical Care, Medical Products Div., Inc. devices

FDA 510(k) Submission Details - K900018

510(k) Number K900018 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 02, 1990
Decision Date July 27, 1990
Days to Decision 206 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
75d slower than avg
Panel avg: 131d · This submission: 206d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KDI Device Classification - Class 2, Special Controls

Product Code KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.5860
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 - KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System

All 298
Devices cleared under the same product code (KDI) and FDA review panel - the closest regulatory comparables to K900018.
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K900918 · Gambro, Inc. · Jul 1990
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K901286 · Amicon, Inc. · May 1990
AMICON MINIFILTER PLUS HEMOFILTER
K895405 · Amicon, Inc. · Jan 1990