Atlas FDA

NOVOSTE BETA-CATH SYSTEM

FDA premarket approval P000018/S027 · decided 2003-10-23

Approval details

PMA number
P000018
Supplement
S027
Supplement type
135 Review Track For 30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
NOVOSTE BETA-CATH SYSTEM
Generic name
Intravascular radiation delivery system
Applicant
Best Vascular, Inc.
Date received
2002-10-21
Decision date
2003-10-23
Days to decision
367 days
Decision code
APPR
Product code
MOU
Advisory committee
Cardiovascular
Expedited review
No
Location
Norcross, GA
Statement
APPROVAL TO CHANGE AN ELECTRONIC DATA MANAGEMENT SYSTEM, REFERRED TO AS THE BETACAL SYSTEM.

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