Atlas FDA

COBAS AMPLICOR CT/NG TEST FOR CHLAMYDIA TRACHOMATIS

FDA 510(k) clearance K053287 · decided 2006-08-10

Clearance details

K-number
K053287
Device name
COBAS AMPLICOR CT/NG TEST FOR CHLAMYDIA TRACHOMATIS
Applicant
Roche Diagnostics Corp.
Decision
Substantially Equivalent
Date received
2005-11-25
Decision date
2006-08-10
Days to decision
258 days
Clearance type
Traditional
Product code
MKZ
Device class
1
Regulation number
866.3120
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Indianapolis, IN, US
Third-party review
No
Expedited review
No

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AMPLICOR CT/NG TEST FOR CHLAMYDIA TRACHOMATIS; ROCHE SCRIPTS FOR CT/NG TEST ACCESSORY (K070174)Roche Diagnostics Corporation2007-04-16
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Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

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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
Elecsys Anti-HBc IgM and PreciControl Anti-HBc IgM (P110031/S025)Roche Diagnostics Corp.2024-11-22