Cleared Traditional

K974798 - STERICHEK(TM) RESIDUAL PEROXIDE REAGENT STRPS

K974798 is an FDA 510(k) clearance for STERICHEK(TM) RESIDUAL PEROXIDE REAGENT..., manufactured by Environmental Test Systems, Inc.. The device is a Class 2 Gastroenterology & Urology device with product code LIF cleared through the Traditional 510(k) pathway after a 88-day FDA review.

K974798 · Environmental Test Systems, Inc. · Gastroenterology & Urology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Mar 1998
Decision
88d
Days
Class 2
Risk

K974798 is an FDA 510(k) clearance for the STERICHEK(TM) RESIDUAL PEROXIDE REAGENT STRPS. Classified as Dialyzer Reprocessing System (product code LIF), Class II - Special Controls.

Submitted by Environmental Test Systems, Inc. (Elkhart, US). The FDA issued a Cleared decision on March 20, 1998 after a review of 88 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 Environmental Test Systems, Inc. devices

FDA 510(k) Submission Details - K974798

510(k) Number K974798 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 22, 1997
Decision Date March 20, 1998
Days to Decision 88 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
43d faster than avg
Panel avg: 131d · This submission: 88d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

LIF Device Classification - Class 2, Special Controls

Product Code LIF Dialyzer Reprocessing System
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 - LIF Dialyzer Reprocessing System

All 32
Devices cleared under the same product code (LIF) and FDA review panel - the closest regulatory comparables to K974798.
AMUKIN D
K992016 · Amuchina Intl., Inc. · Jan 2000
RENACLEAR DIALYZER CLEANING SYSTEM
K991851 · Minntech Corp. · Aug 1999
POTENCY TEST STRIPS, INDICATOR TEST STRIPS
K974426 · Reprocessing Products Corp · Feb 1999
ALEXANDER MANUFACTURING RECHARGEABLE BATTERY (M1/T)
K970799 · Alexander Mfg. Co. · May 1997
DPS 4 DIALYZER PREPARATION SYSTEM
K955299 · Seratronics, Inc. · Oct 1996
DRS 4 DIALYZER REPROCESSING SYSTEM
K931336 · Seratronics, Inc. · Apr 1996