Atlas FDA

Elecsys HBeAg

FDA premarket approval P130015/S020 · decided 2024-08-29

Approval details

PMA number
P130015
Supplement
S020
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Elecsys HBeAg
Generic name
Test, Hepatitis B (B Antigen, B Surface Antigen, Be Antigen)
Applicant
Roche Diagnostics Operations, Inc.
Date received
2024-08-02
Decision date
2024-08-29
Days to decision
27 days
Decision code
OK30
Product code
LOM
Advisory committee
Microbiology
Expedited review
No
Location
Indianapolis, IN
Statement
two additional fill lines

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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