Atlas FDA

AIA-PACK PSA

FDA premarket approval P910065/S009 · decided 2019-06-18

Approval details

PMA number
P910065
Supplement
S009
Supplement type
Special (Immediate Track)
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
AIA-PACK PSA
Generic name
Total, prostate specific antigen (noncomplexed & complexed) for detection of prostate cancer
Applicant
Tosoh Bioscience, Inc.
Date received
2019-05-20
Decision date
2019-06-18
Days to decision
29 days
Decision code
APPR
Product code
MTF
Advisory committee
Immunology
Expedited review
No
Location
South San Franciso, CA
Statement
Approval for labeling changes to the Tosoh AIA-PACK PSA Test to reflect newly acquired information that enhances the safety of the device as allowed by 21 CFR 814.39(d).

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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