FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

DORNIER COMPACT ALPHA LITHOTRIPTER

K Number: K002929 · Decision Apr 17, 2001
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
53
Applicant Total
29
Review Days
209

Basic Information

Device Name
DORNIER COMPACT ALPHA LITHOTRIPTER
K Number
K002929
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5990
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
DORNIER MEDTECH AMERICA, INC.
Date Received
September 20, 2000
Decision Date
April 17, 2001
Product Code
LNS
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

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

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