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DURASPHERE INECTABLE BULKING AGENT

FDA premarket approval P980053/S014 · decided 2013-03-21

Approval details

PMA number
P980053
Supplement
S014
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
DURASPHERE INECTABLE BULKING AGENT
Generic name
AGENT, BULKING, INJECTABLE FOR GASTRO-UROLOGY USE
Applicant
Carbon Medical Technologies, Inc.
Date received
2013-02-19
Decision date
2013-03-21
Days to decision
30 days
Decision code
OK30
Product code
LNM
Advisory committee
Gastroenterology, Urology
Expedited review
No
Location
St. Paul, MN
Statement
MODIFICATION TO THE FOIL POUCH SEALER, AND THE ADDITION OF TWO ALTERNATE SEALERS, AND TWO NEW LABEL PRINTING SYSTEMS.

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