Atlas FDA

HERCEP TEST

FDA premarket approval P980018/S005 · decided 2005-12-30

Approval details

PMA number
P980018
Supplement
S005
Supplement type
Special (Immediate Track)
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
2005-12-08
Decision date
2005-12-30
Days to decision
22 days
Decision code
APPR
Product code
MVC
Advisory committee
Pathology
Expedited review
No
Location
Singapore
Statement
APPROVAL FOR CHANGES IN QUALITY CONTROL STEPS.

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