510(k) K003417

Device
MINI FIBER ENDOSCOPES; OUTER SHEATHS; VERESS CANNULAS; VERESS CANNULAS WITH OUTER SHEATHS, SET
Applicant
Richard Wolf Medical Instruments Corp.
510(k) number
K003417
Product code
HET
Decision
Substantially Equivalent (SESE)
Decision date
2001-04-04
Date received
2000-11-02
Regulation
884.1720
Classification name
Laparoscope, Gynecologic (And Accessories)
Medical specialty
Obstetrics/Gynecology
Review panel
Obstetrics/Gynecology
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
N

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

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