Atlas FDA

Elecsys Anti-HBe

FDA premarket approval P190005/S005 · decided 2024-08-29

Approval details

PMA number
P190005
Supplement
S005
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Elecsys Anti-HBe
Generic name
Test, Hepatitis B (B Antigen, B Surface Antigen, Be Antigen)
Applicant
Roche Diagnostics
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
cobas pulse blood glucose monitoring system (K252323)Roche Diagnostics2026-06-12
Elecsys Anti-SARS-CoV-2 S (K252280)Roche Diagnostics2026-04-13
Elecsys Anti-HBc IgM (K260049)Roche Diagnostics2026-04-07
Elecsys Anti-HBc II (K260046)Roche Diagnostics2026-04-07
Elecsys Anti-HAV IgM (K260048)Roche Diagnostics2026-04-07
Tina-quant Cardiac high sensitivity CRP III (K260026)Roche Diagnostics2026-04-02
Glucose HK Gen.3; ONLINE DAT Methadone II; cobas pro integrated solutions (K253490)Roche Diagnostics2026-02-12
ISE indirect K for Gen.2; ISE indirect Na for Gen.2; ISE indirect Cl for Gen.2; cobas pro integrated solutions (K253491)Roche Diagnostics2026-02-12