Atlas FDA

UROLUME ENDOPROSTHESIS

FDA premarket approval P920023 · decided 1996-05-06

Approval details

PMA number
P920023
Trade name
UROLUME ENDOPROSTHESIS
Generic name
STENT, URETHRAL, BULBOUS, PERMANENT OR SEMI-PERMANENT
Applicant
Boston Scientific Corp
Date received
1992-05-12
Decision date
1996-05-06
Days to decision
1455 days
Decision code
APWD
Product code
MES
Advisory committee
Gastroenterology, Urology
Expedited review
No
Location
Marlboro, MA
Statement
APPROVAL FOR THE UROLUME ENDORETHRAL PROSTHESIS FOR URETHRAL STRICTURES (REFERRED TO AS UROLUME HEREINAFTER)

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510(k) clearances by this applicant

RecordFirmDate
IceSeed 1.5 CX Straight Needle (H7493968333170); IceSphere1.5 CX Straight Needle (H7493968435730); IceRod 1.5 CX Straight Needle (H7493968535330) (K243245)Boston Scientific Corp2024-10-18
LUX-Dx II (M302); LUX-Dx II+ (M312) (K231328)Boston Scientific Corp2023-08-19
WALLSTENT RP Endoprosthesis Transhepatic Biliary, WALLSTENT Endoprosthesis Transhepatic Biliary (K152853)Boston Scientific Corp2015-11-20
AXIOS Stent with Electrocautery Enhanced Delivery System (K150692)Boston Scientific Corp2015-08-05
XXL Vascular Balloon Dilatation Catheter (K150303)Boston Scientific Corp2015-06-15
Chariot Guiding Sheath (K150186)Boston Scientific Corp2015-06-05
EndoVive Initial Placement Standard PEG Kit with ENFit Connector, EndoVive Initial Placement Safety PEG Kit with ENFit Connector (K150679)Boston Scientific Corp2015-05-29
JAGWIRE HIGH PERFORMANCE GUIDWIRE (K141820)Boston Scientific Corp2014-10-21