Cleared Traditional

K902837 - AMICON DIAFILTER 30 HEMOCONCENTRATOR

K902837 is the FDA 510(k) clearance for AMICON DIAFILTER 30 HEMOCONCENTRATOR by Amicon, Inc.. It is a Class 2 Gastroenterology & Urology device (product code KDI) cleared through the Traditional 510(k) pathway after a 126-day FDA review.

K902837 · Amicon, Inc. · Gastroenterology & Urology device
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Nov 1990
Decision
126d
Days
Class 2
Risk

K902837 is an FDA 510(k) clearance for the AMICON DIAFILTER 30 HEMOCONCENTRATOR. Classified as Dialyzer, High Permeability With Or Without Sealed Dialysate System (product code KDI), Class II - Special Controls.

Submitted by Amicon, Inc. (Danvers, US). The FDA issued a Cleared decision on November 1, 1990 after a review of 126 days - within the typical 510(k) review window.

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 Amicon, Inc. devices

Submission Details

510(k) Number K902837 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 28, 1990
Decision Date November 01, 1990
Days to Decision 126 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
4d faster than avg
Panel avg: 130d · This submission: 126d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

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 199
Devices cleared under the same product code (KDI) and FDA review panel - the closest regulatory comparables to K902837.
INPERSOL CAPD BIOCAP ADMINISTRATION SET
K911094 · Abbott Laboratories · Apr 1991
RENAFLO HDF 1350 HEMODIAFILTER
K910236 · Minntech Corp. · Apr 1991
QUICK PRIME HEMOCONCEN. NO. HQ-7000 AND CBP-7000Q
K903641 · Bentley Laboratories, Inc. · Nov 1990
HOLLOW FIBER DIALYZER, BIO CARE PS 130
K900018 · National Medical Care, Medical Products Div., Inc. · Jul 1990
GAMBRO LUNDIA IC-6H PARALLEL PLATE DIALYZER
K900918 · Gambro, Inc. · Jul 1990
HOLLOW FIBER DIALYZER SERIES FOCUS 160/160H
K895759 · National Medical Care, Medical Products Div., Inc. · Nov 1989