RICHARD WOLF PIEZOLITH E.L.P. LITHOTRIPT MODEL2300

FDA Premarket Approval P890013

Pre-market Approval Supplement Details

DeviceRICHARD WOLF PIEZOLITH E.L.P. LITHOTRIPT MODEL2300
Generic NameLithotriptor, Extracorporeal Shock-wave, Urological
ApplicantRICHARD WOLF MEDICAL INSTRUMENTS CORP.
Date Received1989-03-07
Decision Date1991-09-09
Notice Date1991-10-10
PMAP890013
SupplementS
Product CodeLNS 
Docket Number91M-0368
Advisory CommitteeGastroenterology/Urology
Expedited ReviewNo
Combination Product No
Applicant Address RICHARD WOLF MEDICAL INSTRUMENTS CORP. 353 Corporate Woods Pkwy. vernon Hills, IL 60061

Supplemental Filings

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Supplement NumberDateSupplement Type
P890013Original Filing

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