Atlas FDA

DEFLUX INJECTABLE GEL

FDA premarket approval P000029/S041 · decided 2008-04-08

Approval details

PMA number
P000029
Supplement
S041
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
DEFLUX INJECTABLE GEL
Generic name
AGENT, BULKING, INJECTABLE FOR GASTRO-UROLOGY USE
Applicant
Palette Life Sciences
Date received
2008-03-10
Decision date
2008-04-08
Days to decision
29 days
Decision code
OK30
Product code
LNM
Advisory committee
Gastroenterology, Urology
Expedited review
No
Location
Santa Barbara, CA
Statement
CHANGE IN VENT FILTER FOR THE HOLDING TANKS AND A NEW TEST METHOD FOR INTEGRITY TESTING.

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.

510(k) clearances by this applicant

RecordFirmDate
Barrigel Injectable Gel (K220641)Palette Life Sciences2022-05-26