MDI ACTUATOR MANUFACTURED BY BALLARD MEDICAL PRODUCTS

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Request for Information Form	Contact Information
Company Name	BALLARD MEDICAL PRODUCTS
Address	12050 LONE PEAK PKWY.
City, State, Zip	DRAPER, UT 84020
Country	US
FDA Owner/Operator Phone	972-281-1200
FDA Medical Specialty Code	EN - Ear, Nose, Throat
FDA Product Code	LRD
FDA Classification Name	APPLICATOR, ENT DRUG
FDA Device Classification Code	General Controls
FDA Regulation Number	874.5220
FDA Common Generic Name	MDI ACTUATOR
FDA Proprietary Device Name	MDI ACTUATOR
FDA Owner / Operator Number	9001775
FDA Owner / Operator Name	KIMBERLY-CLARK CORP.
FDA Establishment Registration Number	1719891
FDA Registered Establishment Name	BALLARD MEDICAL PRODUCTS
FDA Operation Code(s)	MS - Specification Developer
FDA Listing Date	12-22-99
FDA Listing Status Code	Active
Differentiation	N/A
Keywords	N/A
Description	N/A
Brochure	N/A
Product Website	N/A

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