FDA PMA FDA Class 2 Approved 🇺🇸 United States

Lithotriptor, Extracorporeal Shock-Wave, Urological

PMA: P890066 · Supplement: S004 · Decision Mar 26, 1992
Classifications
1
FEI Numbers
17
Registration Numbers
17

Basic Information

Device Name
Lithotriptor, Extracorporeal Shock-Wave, Urological
Trade Name
THERASONIC LITHOTRIPSY TREATMENT SYSTEM
PMA Number
P890066
Supplement Number
S004
Device Class
FDA Class 2
Product Code
LNS
Generic Name
Lithotriptor, extracorporeal shock-wave, urological
Regulation Number
876.5990
Medical Specialty
Gastroenterology, Urology
Advisory Committee
Gastroenterology, Urology
Decision
Approved
Decision Code
APPR
Decision Date
March 26, 1992
Date Received
March 10, 1992
Supplement Type
Normal 180 Day Track
Supplement Reason
Other
Expedited Review
N

Classifications

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

Product Code Device Name
LNS Lithotriptor, Extracorporeal Shock-Wave, Urological