Atlas FDA

BETA-CATH(TM) SYSTEM

FDA premarket approval P000018/S014 · decided 2001-07-13

Approval details

PMA number
P000018
Supplement
S014
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
BETA-CATH(TM) SYSTEM
Generic name
Intravascular radiation delivery system
Applicant
Best Vascular, Inc.
Date received
2001-06-14
Decision date
2001-07-13
Days to decision
29 days
Decision code
OK30
Product code
MOU
Advisory committee
Cardiovascular
Expedited review
No
Location
Norcross, GA
Statement
CHANGE IN THE STERILIZATION PROCESS.

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