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DURASPHERE INJECTABLE BULKING AGENT

FDA premarket approval P980053/S002 · decided 2001-01-23

Approval details

PMA number
P980053
Supplement
S002
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
DURASPHERE INJECTABLE BULKING AGENT
Generic name
AGENT, BULKING, INJECTABLE FOR GASTRO-UROLOGY USE
Applicant
Carbon Medical Technologies, Inc.
Date received
2001-01-09
Decision date
2001-01-23
Days to decision
14 days
Decision code
OK30
Product code
LNM
Advisory committee
Gastroenterology, Urology
Expedited review
No
Location
St. Paul, MN
Statement
ADDITION OF AN ALTERNATE VENDOR, CARBON COATING TECHNOLOGIES, TO SUPPLY THE PYLORIC CARBON COATED BEAD COMPONENT OF THE DURASPHERE INJECTABLE BULKING AGENT(R)

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