FDA 510(k) Applications Submitted by INSTRUMENTARIUM CORP.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K955018	11/02/1995	TRIP NGS & SIGMOID CATHETER PHI SLIDE CALCULATOR	INSTRUMENTARIUM CORP.
K001729	06/07/2000	FOCUS	INSTRUMENTARIUM CORP.
K962638	07/05/1996	TONOCAP, TC-200 AND ACCESSORY CATHETERS	INSTRUMENTARIUM CORP.
K961441	04/15/1996	TONOMETERED SLAINE BLOOD GAS CONTROL	INSTRUMENTARIUM CORP.
K022630	08/07/2002	MODIFICATION TO FOCUS	INSTRUMENTARIUM CORP.
K981641	05/08/1998	MAMMOGRAPHY X-RAY EQUIPMENT MODELS MGF101 AND MGF110, ALPHA III, ALPHA ST, ALPHA RT AND ALPHA IQ	INSTRUMENTARIUM CORP.
K001439	05/08/2000	ORTHOCEPH OC100 D	INSTRUMENTARIUM CORP.
K992385	07/16/1999	ORTHOPANTOMOGRAPH OP100D	INSTRUMENTARIUM CORP.