TECHNOMED INTERNATIONAL SONOLITH 2000

Lithotriptor, Extracorporeal Shock-wave, Urological

FDA Premarket Approval P880011

This medical device has supplements. The device description/function or indication may have changed. Be sure to look at the supplements to get an up-to-date information on device changes. The labeling included below is the version at time of approval of the original pma or panel track supplement and may not represent the most recent labeling.

Pre-market Approval Supplement Details

DeviceTECHNOMED INTERNATIONAL SONOLITH 2000
Classification NameLithotriptor, Extracorporeal Shock-wave, Urological
Generic NameLithotriptor, Extracorporeal Shock-wave, Urological
ApplicantEDAP INTERNATIONAL CORP.
Date Received1988-02-18
Decision Date1989-06-23
Notice Date1989-07-19
PMAP880011
SupplementS
Product CodeLNS
Docket Number89M-0211
Advisory CommitteeGastroenterology/Urology
Expedited ReviewNo
Combination Product No
Applicant Address EDAP INTERNATIONAL CORP. two Burlington Woods burlington, MA 01803

Supplemental Filings

Supplement NumberDateSupplement Type
P880011Original Filing
S009 1997-10-29 Special (immediate Track)
S008 1994-03-08 Normal 180 Day Track
S007 1991-11-01 Normal 180 Day Track
S006
S005
S004 1990-09-24 Normal 180 Day Track
S003 1990-09-11 Normal 180 Day Track
S002 1989-04-28 Normal 180 Day Track
S001 1989-04-05 Normal 180 Day Track

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