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510(k) Premarket Notification Database

Device Classification Name:	IMAGE DIGITIZER
Regulation Number:	892.2030 [See Other Products with this regulation number]
510(k) Number:	K032022
Device Name:	DIGITAL IMAGER
Applicant:	PYRAMID MEDICAL, INC. 10940 PORTAL MEDICAL DR. LOS ALAMITOS, CA 90720
Contact:	CLAUDE BENNETT
Product Code:	LMA [See Other Manufacturers that make this Product]
Date Received:	06-30-2003
Decision Date:	09-02-2003
Decision:	SE
Advisory Committee:	RA
Statement/Summary/Purged Status:	Statement
Type:	Traditional
Review by Third Party:	N
Expedited Review:	N

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