TEST, SPECTACLE DISSOCIATION, BATTERY-POWERED (LANCASTER) MANUFACTURED BY GULDEN OPHTHALMICS

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Request for Information Form	Contact Information
Company Name	GULDEN OPHTHALMICS
Address	225 CADWALADER AVE.
City, State, Zip	ELKINS PARK, PA 19027
Country	US
FDA Owner/Operator Phone	215-884-8105 201
FDA Medical Specialty Code	OP - Opthalmic
FDA Product Code	HLO
FDA Classification Name	TEST, SPECTACLE DISSOCIATION, BATTERY-POWERED (LANCASTER)
FDA Device Classification Code	General Controls
FDA Regulation Number	886.1910
FDA Common Generic Name	SPECTACLE DISSOCIATION TEST
FDA Proprietary Device Name	TEST, SPECTACLE DISSOCIATION, BATTERY-POWERED (LANCASTER)
FDA Owner / Operator Number	2518410
FDA Owner / Operator Name	GULDEN OPHTHALMICS
FDA Establishment Registration Number	2518410
FDA Registered Establishment Name	GULDEN OPHTHALMICS
FDA Operation Code(s)	MM - Manufacturer
FDA Listing Date	03-12-95
FDA Listing Status Code	Active
Differentiation	N/A
Keywords	N/A
Description	N/A
Brochure	N/A
Product Website	N/A