Atlas FDA

Elecsys Anti-HBs

FDA premarket approval P010054/S032 · decided 2017-12-20

Approval details

PMA number
P010054
Supplement
S032
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
Elecsys Anti-HBs
Generic name
Test, Hepatitis B (B Antigen, B Surface Antigen, Be Antigen)
Applicant
Roche Diagnostics Corp.
Date received
2017-10-11
Decision date
2017-12-20
Days to decision
70 days
Decision code
APPR
Product code
LOM
Advisory committee
Microbiology
Expedited review
No
Location
Indianapolis, IN
Statement
Approval for implementation of system software 06-04 on the cobas e 602 to address a software limitation

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510(k) clearances by this applicant

RecordFirmDate
SUPER SANI-CLOTH/ ACCU-CHEK INFORM II SYSTEM (K130138)Roche Diagnostics Corp.2013-03-15
ELECSYS CA 19-9 CALCHECK 5 (K101365)Roche Diagnostics Corp.2010-10-05
COBAS 8000 MODULAR SERIES ANALYZER (K100853)Roche Diagnostics Corp.2010-09-09
ACCU-CHEK ULTRFLEX INFUSION SET (K101196)Roche Diagnostics Corp.2010-08-27
AMPHETAMINES II ASSAY (K093664)Roche Diagnostics Corp.2010-07-28
ELECSYS INSULIN CALCHECK 5 (K101075)Roche Diagnostics Corp.2010-06-11
ELECSYS TESTOSTERONE II IMMUNOASSAY (K093421)Roche Diagnostics Corp.2010-04-23
ELECSYS TROPONIN T CALCHECK 5 (K092848)Roche Diagnostics Corp.2010-03-19