Atlas FDA

NOVOSTE TM BETA-CATH TM SYSTEM

FDA premarket approval P000018/S030 · decided 2003-02-26

Approval details

PMA number
P000018
Supplement
S030
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
NOVOSTE TM BETA-CATH TM SYSTEM
Generic name
Intravascular radiation delivery system
Applicant
Best Vascular, Inc.
Date received
2003-02-07
Decision date
2003-02-26
Days to decision
19 days
Decision code
OK30
Product code
MOU
Advisory committee
Cardiovascular
Expedited review
No
Location
Norcross, GA
Statement
ALTERNATE METHOD OF MANUFACTURE FOR THE LEAK TESTING AND DRYING OPERATION OF THE BETA-RAIL 3.5F DELIVERY CATHETER.

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