Atlas FDA

ROCHE DIAGNOSTICS TINA-QUANT IGM GEN.2

FDA 510(k) clearance K040431 · decided 2004-03-10

Clearance details

K-number
K040431
Device name
ROCHE DIAGNOSTICS TINA-QUANT IGM GEN.2
Applicant
Roche Diagnostics Corp.
Decision
Substantially Equivalent
Date received
2004-02-19
Decision date
2004-03-10
Days to decision
20 days
Clearance type
Special
Product code
DAO
Device class
2
Regulation number
866.5550
Medical specialty
Immunology
Advisory committee
Immunology
Location
Indianapolis, IN, US
Third-party review
No
Expedited review
No

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Recalls involving this device

RecordFirmDate
Tina-quant IgM Gen.2, Catalog Nos. 03507190190, 05220726190, 03507041190, 03507149190 Prod recall (Z-1147-2019)Roche Diagnostics Corporation2019-04-13

PMA approvals by this applicant

RecordFirmDate
ELECSYS FREE PSA IMMUNOASSAY/CALSET/CALCHECK (P000027/S043)Roche Diagnostics Corp.2025-05-27
ELECSYS TOTAL PSA IMMUNOASSAY AND TOTAL PSA CALSET (P990056/S044)Roche Diagnostics Corp.2025-05-27
Elecsys Anti-HBc II (P100031/S033)Roche Diagnostics Corp.2025-05-22
Elecsys Anti-HBc II (P100032/S023)Roche Diagnostics Corp.2025-05-22
Elecsys Anti-HBc IgM (P110031/S027)Roche Diagnostics Corp.2025-05-22
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