510(k) K920235

Device
Ultrasound Generator Modle 2270
Applicant
RICHARD WOLF MEDICAL INSTRUMENTS CORP.
510(k) number
K920235
Product code
FEO
Decision
Substantially Equivalent (SESE)
Decision date
1992-12-07
Date received
1992-01-17
Regulation
876.4480
Classification name
Lithotriptor, Ultrasonic
Medical specialty
Gastroenterology, Urology
Review panel
Gastroenterology, Urology
Device class
2
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
No

Applicant Contact#

Contact
ROBERT L CASARSA
Address
353 Corporate Woods Pkwy. Vernon Hills IL US 60061 60061

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

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