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VIDAS FREE PSA RT

FDA premarket approval P080008/S002 · decided 2013-01-18

Approval details

PMA number
P080008
Supplement
S002
Supplement type
Real-Time Process
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
VIDAS FREE PSA RT
Generic name
Test, prostate specific antigen, free, (noncomplexed) to distinguish prostate cancer from benign conditions
Applicant
bioMerieux, Inc.
Date received
2012-10-11
Decision date
2013-01-18
Days to decision
99 days
Decision code
APPR
Product code
MTG
Advisory committee
Immunology
Expedited review
No
Location
Hazelwood, MO
Statement
APPROVAL FOR UPDATING THE PACKAGING INSERT BY DEFINING THE PHRASE"INSTRUMENT OF THE VIDAS FAMILY" AS "INSTRUMENT OF THE VIDAS FAMILY: VIDAS OR MINIVIDAS"AND REPLACING "INSTRUMENTS OF THE VIDAS FAMILY" WITH "VIDAS INSTRUMENTS" IN THEINTENDED USE. THE DEVICE, VIDAS® TOTAL PSA, IS INTENDED FOR USE WITH THE VIDAS INSTRUMENTS(VITEK® IMMUNODIAGNOSTIC ASSAY SYSTEM) AS AN AUTOMATED ENZYME-LINKED FLUORESCENTIMMUNOASSAY (ELFA) FOR THE QUANTITATIVE MEASUREMENT OFTOTAL PROSTATE SPECIFIC ANTIGEN IN HUMAN SER

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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