Atlas FDA

VIDAS TOTAL PSA ASSAY

FDA premarket approval P040008/S012 · decided 2015-08-05

Approval details

PMA number
P040008
Supplement
S012
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
VIDAS TOTAL PSA ASSAY
Generic name
Total, prostate specific antigen (noncomplexed & complexed) for detection of prostate cancer
Applicant
bioMerieux, Inc.
Date received
2015-07-06
Decision date
2015-08-05
Days to decision
30 days
Decision code
OK30
Product code
MTF
Advisory committee
Immunology
Expedited review
No
Location
Hazelwood, MO
Statement
ADDITION OF AN ALTERNATE QUALIFIED SUPPLIER FOR THE VIDAS STRIPS.

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510(k) clearances by this applicant

RecordFirmDate
VITEK REVEAL GN AST Assay and VITEK REVEAL AST System (K260160)bioMerieux, Inc.2026-07-08
VITEK 2 AST-Streptococcus Inducible Clindamycin Resistance (K260282)bioMerieux, Inc.2026-04-15
VITEK 2 AST-Gram Negative Cefazolin (=<1-=>32 µg/mL) (K251579)bioMerieux, Inc.2025-08-21
VITEK COMPACT PRO (K234012)bioMerieux, Inc.2025-03-14
VITEK 2 AST-Yeast Voriconazole (<= 0.03125 - >= 4 µg/mL) (K232967)bioMerieux, Inc.2024-06-12
VITEK 2 AST-Yeast Anidulafungin (<= 0.015 - >= 8 µg/mL) (K232963)bioMerieux, Inc.2024-06-07
VIDAS TBI (GFAP, UCH-L1) (K240279)bioMerieux, Inc.2024-05-01
VITEK 2 AST-Gram Positive Lefamulin (<=0.03 - >=4 µg/mL) (K234000)bioMerieux, Inc.2024-03-11