Atlas FDA

URISYS 2400 URINE TEST STRIP

FDA 510(k) clearance K012397 · decided 2001-09-26

Clearance details

K-number
K012397
Device name
URISYS 2400 URINE TEST STRIP
Applicant
Roche Diagnostics Corp.
Decision
Substantially Equivalent
Date received
2001-07-27
Decision date
2001-09-26
Days to decision
61 days
Clearance type
Traditional
Product code
JIL
Device class
2
Regulation number
862.1340
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
Indianapolis, IN, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

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iChemVELOCITY Automated Urine Chemistry System (K171083)Iris Diagnostics, A Division of Iris International, Inc.2017-05-12
AUTION ELEVEN Semi-Automated Urinalysis System (K160062)Arkray, Inc.2016-10-07
URITEK TC-201 URINE CHEMISTRY TEST SYSTEM (K160372)Teco Diagnostics, Inc.2016-07-22
TC-THUNDERBOLT AUTOMATED URINE ANALYZER SYSTEM AND TC-THUNDERBOLT URS-10 STRIPS (K141289)Teco Diagnostics2015-07-24
URS-2GP (GLUCOSE PROTEIN) URINE STRIPS (K131600)Teco Diagnostics2014-05-29
FORESIGHT U120 URINE ANALYZER (K120124)ACON Laboratories, Inc.2012-03-06

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

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Elecsys Anti-HBc IgM (P110022/S034)Roche Diagnostics Corp.2025-05-22
Elecsys Anti-HBs (P010054/S048)Roche Diagnostics Corp.2025-05-22
Elecsys Anti-HBc IgM and PreciControl Anti-HBc IgM (P110031/S025)Roche Diagnostics Corp.2024-11-22