Atlas FDA

RENATRON DIALYZER REPROCESSING SYS

FDA 510(k) clearance K830574 · decided 1983-03-29

Clearance details

K-number
K830574
Device name
RENATRON DIALYZER REPROCESSING SYS
Applicant
Renal Systems, Inc.
Decision
Substantially Equivalent
Date received
1983-02-23
Decision date
1983-03-29
Days to decision
34 days
Clearance type
Traditional
Product code
LIF
Device class
2
Regulation number
876.5820
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
CLEARFLUX DIALYZER REPROCESSING SYSTEM (K091360)Novaflux Technologies2010-11-03
ASSIST HEADER CLEANER (K043126)Alcavis International, Inc.2005-02-03
STERICHEK GLUTARALDEHYDE REAGENT STRIPS (K040660)Hach Company2004-11-15
RENACLEAN SH DIALYZER CLEANING SYSTEM (K033505)Minntech Corp.2004-04-27
MAKY 21.1 DIALYZER REPROCESSING SYSTEM (K024076)Hdc Maquinolas, LLC2003-09-26
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
STERICHEK(TM) RESIDUAL PEROXIDE REAGENT STRPS (K974798)Environmental Test Systems, Inc.1998-03-20
ALEXANDER MANUFACTURING RECHARGEABLE BATTERY (M1/T) (K970799)Alexander Mfg. Co.1997-05-14
DPS 4 DIALYZER PREPARATION SYSTEM (K955299)Seratronics, Inc.1996-10-21

Recalls involving this device

No recalls on record reference this clearance.