Atlas FDA

Elecsys HBcAg

FDA premarket approval P130015/S015 · decided 2018-06-13

Approval details

PMA number
P130015
Supplement
S015
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
Elecsys HBcAg
Generic name
Test, Hepatitis B (B Antigen, B Surface Antigen, Be Antigen)
Applicant
Roche Diagnostics Operations, Inc.
Date received
2018-04-17
Decision date
2018-06-13
Days to decision
57 days
Decision code
APPR
Product code
LOM
Advisory committee
Microbiology
Expedited review
No
Location
Indianapolis, IN
Statement
Approval for a software update (version 06-05) for the cobas 8000 Modular Analyzer Series

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510(k) clearances by this applicant

RecordFirmDate
ACCU-CHEK AVIVA EXPERT BLOOD GLUCOSE MONITORING SYSTEM (K131366)Roche Diagnostics Operations, Inc.2013-10-11
ACCU-CHEK AVIVA PLUS TEST STRIP (K131029)Roche Diagnostics Operations, Inc.2013-08-09