Atlas FDA

Hercep Test

FDA premarket approval P980018/S024 · decided 2018-02-08

Approval details

PMA number
P980018
Supplement
S024
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Hercep Test
Generic name
SYSTEM, TEST, HER-2/NEU, IHC
Applicant
Agilent Technologies Singapore (International) Pte , Ltd.
Date received
2018-01-12
Decision date
2018-02-08
Days to decision
27 days
Decision code
OK30
Product code
MVC
Advisory committee
Pathology
Expedited review
No
Location
Singapore
Statement
Changes to the manufacturing process of a buffer.

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