Atlas FDA

ST AIA-PACK PA

FDA premarket approval P910065/S001 · decided 1999-09-10

Approval details

PMA number
P910065
Supplement
S001
Supplement type
Panel Track
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
ST AIA-PACK PA
Generic name
PROSTATE-SPECIFIC ANTIGEN (PSA) FOR MANAGEMENT OF PROSTATE CANCERS
Applicant
Tosoh Bioscience, Inc.
Date received
1999-03-25
Decision date
1999-09-10
Days to decision
169 days
Decision code
APPR
Product code
LTJ
Advisory committee
Immunology
Expedited review
No
Location
South San Franciso, CA
Statement
Approval for the AIA-PACK PA. The device is designed for in vitro diagnostic use only for the quantitative measurement of Prostate Specific Antigen (PSA) in human serum on TOSOH AIA System analyzers. This device is indicated for the measurement of serum PSA in conjunction with Digital Rectal Examination (DRE) as an aid in the detection of prostate cancer (CaP) in men fifty years of age and older. Prostate biopsy is required for the diagnosis of cancer. The device is further indicated for the ser

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510(k) clearances by this applicant

RecordFirmDate
Tosoh Automated Glycohemoglobin Analyzer HLC-723GR01 (K250073)Tosoh Bioscience, Inc.2025-10-03
ST AIA-PACK BNP Assay (K211199)Tosoh Bioscience, Inc.2021-11-08
Tosoh Automated Glycohemoglobin Analyzer HLC-723G8 (K200904)Tosoh Bioscience, Inc.2021-08-05
ST AIA-PACK hsE2 Calibrator Set (K160113)Tosoh Bioscience, Inc.2016-02-17
ST AIA-PACK PROG III Calibrator Set (K153417)Tosoh Bioscience, Inc.2015-12-18
ST AIA-PACK 25-OH Vitamin D, ST AIA-PACK 25-OH Vitamin D Calibrator Set, AIA-PACK 25-OH Vitamin D Control Set, and ST AIA-PACK 25-OH Vitamin D Pretreatment Set (K150270)Tosoh Bioscience, Inc.2015-10-26
ST AIA-PACK SHBG, ST AIA-PACK SHBG Calibrator Set (K143075)Tosoh Bioscience, Inc.2015-07-02
AIA-PACK C-Peptide Control Set (K143296)Tosoh Bioscience, Inc.2014-12-16