Atlas FDA

HERCAP TEST

FDA premarket approval P980018/S016 · decided 2013-02-22

Approval details

PMA number
P980018
Supplement
S016
Supplement type
Normal 180 Day Track
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
HERCAP TEST
Generic name
SYSTEM, TEST, HER-2/NEU, IHC
Applicant
Agilent Technologies Singapore (International) Pte , Ltd.
Date received
2012-08-24
Decision date
2013-02-22
Days to decision
182 days
Decision code
APPR
Product code
MVC
Advisory committee
Pathology
Expedited review
No
Location
Singapore
Statement
APPROVAL FOR ADDITION OF KADCYLA¿ (ADO-TRASTUZUMAB EMTANSINE) IN THE LABELING OF HERCEP TEST ¿.

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.