TECHNOMED INTERNATIONAL SONOLITH 2000

Lithotriptor, Extracorporeal Shock-wave, Urological

FDA Premarket Approval P880011 S004

This medical device record is a pma supplement. A supplement may have changed the device description/function or indication from that approved in the original pma. Be sure to look at the original pma record for more information.

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 Received1990-09-24
Decision Date1990-12-24
PMAP880011
SupplementS004
Product CodeLNS
Advisory CommitteeGastroenterology/Urology
Supplement TypeNormal 180 Day Track
Supplement ReasonOther Report
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

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.