FDA 510(k) Applications Submitted by RADIOMETER AMERICA, INC.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K980130	01/14/1998	ABL700 SERIES BLOOD GAS , CO-OXIMETRY, ELECTROLYTE & METABOLITE SYSTEM	RADIOMETER AMERICA, INC.
K980135	01/15/1998	QUALICHECK5+ MODELS S7730, S7740, S7750, S7760	RADIOMETER AMERICA, INC.
K961354	04/08/1996	QUALICHECK 4 METABOLITE(S3630,S3640,S3650,S3660)	RADIOMETER AMERICA, INC.
K961355	04/08/1996	MULTICHECK	RADIOMETER AMERICA, INC.
K962158	06/04/1996	PICO MODELS 30, 50, 70	RADIOMETER AMERICA, INC.
K952725	06/14/1995	MULTICHECK	RADIOMETER AMERICA, INC.
K962334	06/17/1996	EML105 ELECTROLYTE METABOLITE ANALYZER	RADIOMETER AMERICA, INC.
K973367	09/08/1997	ABL555 BLOOD GAS, ELECTROLYTE & METABOLITE SYSTEM	RADIOMETER AMERICA, INC.
K974818	12/23/1997	ABL555 BLOOD GAS, ELECTROLYTE & METABOLITE SYSTEM	RADIOMETER AMERICA, INC.
K991417	04/23/1999	ABL 735 ANALYZER	RADIOMETER AMERICA, INC.
K982928	08/20/1998	NPT7 SERIES PH/BLOOD GAS AND CO-OXIMETRY SYSTEM	RADIOMETER AMERICA, INC.
K992859	08/25/1999	ABL700 SERIES ANALYZER WITH AUTOCHECK MODULE	RADIOMETER AMERICA, INC.