Atlas FDA

HERCEPTEST

FDA premarket approval P980018/S022 · decided 2016-07-22

Approval details

PMA number
P980018
Supplement
S022
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
HERCEPTEST
Generic name
SYSTEM, TEST, HER-2/NEU, IHC
Applicant
Agilent Technologies Singapore (International) Pte , Ltd.
Date received
2016-06-06
Decision date
2016-07-22
Days to decision
46 days
Decision code
APPR
Product code
MVC
Advisory committee
Pathology
Expedited review
No
Location
Singapore
Statement
Approval for the DakoLink software version 4.1 update for the HercepTest.

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