Atlas FDA

DIA STRIPS SYSTEM, MODIFIED

FDA 510(k) clearance K921495 · decided 1992-07-21

Clearance details

K-number
K921495
Device name
DIA STRIPS SYSTEM, MODIFIED
Applicant
Symcon Intl., Inc.
Decision
Substantially Equivalent
Date received
1992-03-06
Decision date
1992-07-21
Days to decision
137 days
Clearance type
Traditional
Product code
JIO
Device class
2
Regulation number
864.6550
Medical specialty
Hematology
Advisory committee
Hematology
Location
Lenexa, KS, US
Third-party review
No
Expedited review
No

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

RecordFirmDate
UC-1800 Automatic Urine Analyzer, URIT 11FA Urine Reagent Strips, URIT 12FA Urine Reagent Strips (K232317)Urit Medical Electronic Co., Ltd.2024-04-26
HEALGEN 11 REAGENT STRIP FOR URINALYSIS, HEALGEN 10 REAGENT STRIP FOR URINALYSIS, AND HEALGEN 4 REAGENT STRIP FOR URINAL (K111999)Healgen Scientific,, LLC2012-04-17
MISSION U500 URINE ANALYZER (K111221)ACON Laboratories, Inc.2012-01-18
URITEST 10G & 11G URINE REAGENT STRIPS AND URITEST-50 AND URITEST-500B URINE ANALYZERS (K082811)Urit Medical Electronic Co., Ltd.2009-09-11
WIENER LAB. URINE STRIP 10 AND 11 (K083724)Wiener Laboratorios Saic2009-09-02
URISTIK H SERIES REAGENT STRIPS FOR URINALYSIS (K040703)Dirui Industrial Co., Ltd.2004-08-26
URS-1B (BLOOD TEST) (K023297)Teco Diagnostics2003-03-06
BACTIDROP(TM) LACTOPHENOL ANILINE BLUE (K913005)Remel Co.1991-09-16
HEMASTIX REAGENT STRIPS (K905396)Heraeus Kulzer, Inc.1991-02-11
CHARISE CHARLES REAGENT BLOOD STRIPS (K893894)Lee Import Domestic Consulting1989-07-27

Recalls involving this device

No recalls on record reference this clearance.