Atlas FDA

STERICHEK(TM) RESIDUAL PEROXIDE REAGENT STRPS

FDA 510(k) clearance K974798 · decided 1998-03-20

Clearance details

K-number
K974798
Device name
STERICHEK(TM) RESIDUAL PEROXIDE REAGENT STRPS
Applicant
Environmental Test Systems, Inc.
Decision
Substantially Equivalent
Date received
1997-12-22
Decision date
1998-03-20
Days to decision
88 days
Clearance type
Traditional
Product code
LIF
Device class
2
Regulation number
876.5820
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
Elkhart, IN, US
Third-party review
No
Expedited review
No

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ARM AUTOMATIC REPROCESSING MACHINE (K013713)Alcavis International Incorporated2002-07-15
AMUKIN D (K992016)Amuchina Intl., Inc.2000-01-10
RENACLEAR DIALYZER CLEANING SYSTEM (K991851)Minntech Corp.1999-08-30
POTENCY TEST STRIPS, INDICATOR TEST STRIPS (K974426)Reprocessing Products Corp1999-02-10
ALEXANDER MANUFACTURING RECHARGEABLE BATTERY (M1/T) (K970799)Alexander Mfg. Co.1997-05-14
DPS 4 DIALYZER PREPARATION SYSTEM (K955299)Seratronics, Inc.1996-10-21
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Recalls involving this device

RecordFirmDate
HACH SteriChek Residual Peroxide Reagent Strips, 5/100-strip bottles per kit, Kit Part #81 recall (Z-2016-2009)Hach Co2009-09-04