Atlas FDA

BETA-CATH (TM) SYSTEM

FDA premarket approval P000018/S047 · decided 2016-07-26

Approval details

PMA number
P000018
Supplement
S047
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
2016-02-26
Decision date
2016-07-26
Days to decision
151 days
Decision code
OK30
Product code
MOU
Advisory committee
Cardiovascular
Expedited review
No
Location
Norcross, GA
Statement
Use of a new supplier and a change to the Bacterial Endotoxin Test sampling plan.

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