"GOOD I" MANUFACTURED BY DABL TECHNOLOGY, INC.

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This company has been viewed 14 times within the past 60 days.

This product has been viewed: 2 times.

Request for Information Form	Contact Information
Company Name	DABL TECHNOLOGY, INC.
Address	110-07 73 RD., SUITE, #4M
City, State, Zip	FOREST HILLS, NY 11375
Country	US
FDA Owner/Operator Phone	718-793-7362
FDA Medical Specialty Code	GU - Gastroenterology/Urology
FDA Product Code	LST
FDA Classification Name	DEVICE, ERECTILE DYSFUNCTION
FDA Device Classification Code
FDA Regulation Number	NULL
FDA Common Generic Name	PENIS (ERECTILE) MASSEUR
FDA Proprietary Device Name	"GOOD I"
FDA Owner / Operator Number	9031820
FDA Owner / Operator Name	DABL TECHNOLOGY, INC.
FDA Establishment Registration Number	2437686
FDA Registered Establishment Name	DABL TECHNOLOGY, INC.
FDA Operation Code(s)	RR - Repackager/Relabeller
FDA Listing Date	09-29-97
FDA Listing Status Code	Active
Differentiation	N/A
Keywords	N/A
Description	N/A
Brochure	N/A
Product Website	N/A

Our records indicate that the following medical device companies may manufacture a similar device.

	Company Name / Address / Phone	Proprietary Device Name	Common Generic Device Name
1	D. E. HOKANSON, INC. 12840 N.E. 21ST PL. BELLEVUE, WA 98005 US 425-882-1689 / 425-882-1689	DEVICE, ERECTILE DYSFUNCTION	DISPOSABLE DIGIT CUFFS
2	LABORIE MEDICAL TECHNOLOGIES, INC. 6415 NORTHWEST DR., UNIT 11 MISSISSAUGA, L4V 1X1 CA 31-053-4340902 / 802-857-1300	PI-CAV-UPG	CAVENOSOMETRY UPGRADE PACKAGE
3	MEDICAL MEASUREMENT SYSTEMS,B.V. COLOSSEUM 25 ENSCHEDE, 7521 PV NL 315-348-03739 / 315-348-03739	UD 511	CAVERNOSOMETRY OPTION