FDA PMA FDA Class 3 Approved 🇺🇸 United States

Catheter, Balloon, Urethral, Drug-Coated

PMA: P210020 · Supplement: S002 · Decision Jan 27, 2022
Classifications
1
FEI Numbers
2
Registration Numbers
2

Basic Information

Device Name
Catheter, Balloon, Urethral, Drug-Coated
Trade Name
Optilume Urethral Drug Coated Balloon
PMA Number
P210020
Supplement Number
S002
Device Class
FDA Class 3
Product Code
QRH
Generic Name
Catheter, Balloon, Urethral, Drug-Coated
Medical Specialty
Unknown
Advisory Committee
Gastroenterology, Urology
Decision
Approved
Decision Code
APPR
Decision Date
January 27, 2022
Date Received
December 28, 2021
Supplement Type
Normal 180 Day Track No User Fee
Supplement Reason
Postapproval Study Protocol
Expedited Review
N

Advisory Committee Statement

Approval of the protocol for the post-approval study (PAS) protocol.

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
QRH Catheter, Balloon, Urethral, Drug-Coated