Atlas FDA

ELECSYS TESTOSTERONE II IMMUNOASSAY

FDA 510(k) clearance K093421 · decided 2010-04-23

Clearance details

K-number
K093421
Device name
ELECSYS TESTOSTERONE II IMMUNOASSAY
Applicant
Roche Diagnostics Corp.
Decision
Substantially Equivalent
Date received
2009-11-03
Decision date
2010-04-23
Days to decision
171 days
Clearance type
Traditional
Product code
CDZ
Device class
1
Regulation number
862.1680
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
Indianapolis, IN, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
ELECSYS FREE PSA IMMUNOASSAY/CALSET/CALCHECK (P000027/S043)Roche Diagnostics Corp.2025-05-27
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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
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