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510(k) K883760

Device
STORZ MODEL 62 ENT CAMERA SYSTEM
Applicant
STORZ INSTRUMENT CO.
510(k) number
K883760
Product code
FWL  
Decision
Substantially Equivalent (SESE)
Decision date
1988-09-28
Date received
1988-09-06
Regulation
878.4160
Classification name
Camera, Cine, Endoscopic, Without Audio
Medical specialty
General & Plastic Surgery
Review panel
General & Plastic Surgery
Device class
1
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
DAN REGAN
Address
3365 Tree Ct. Industrial Blvd. St. Louis MO US 63122 63122

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code FWL  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K951519WECO ENDOSCOPIC SYSTEM WITH FIBER OPTIC LIGHTWells Johnson Co.1995-06-14

Legacy Summary#

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FDA Review#

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