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510(k) Premarket Notification Database

Device Classification Name:	TELESCOPE, RIGID, ENDOSCOPIC
Regulation Number:	876.1500 [See Other Products with this regulation number]
510(k) Number:	K031758
Device Name:	ACMI M4 TELESCOPES
Applicant:	ACMI CORPORATION 136 TURNPIKE RD. SOUTHBOROUGH, MA 01772 2104
Contact:	GABRIEL J MURACA
Product Code:	FBP [See Other Manufacturers that make this Product]
Date Received:	06-06-2003
Decision Date:	09-02-2003
Decision:	SE
Advisory Committee:	GU
Statement/Summary/Purged Status:	Summary
Type:	Traditional
Review by Third Party:	N
Expedited Review:	N

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