FDA 510(k) Applications Submitted by BETTY LANE

FDA 510(k) Number Submission Date Device Name Applicant
K850136 01/14/1985 CARDIO DATA MK4 HOLTER ANALYSIS SYSTEM CARDIO DATA
K860167 01/17/1986 PRODIGY AND PRODIGY PLUS CARDIODATA CORP.
K881488 04/08/1988 HOLTER SCANNER CARDIODATA CORP.
K853262 08/05/1985 CARDIO DATA PACERECORDER PR3 CARDIO DATA
K873337 08/19/1987 MODEL SSR1 HOLTER MONITOR CARDIODATA CORP.
K983468 10/01/1998 FASTTAKE ADAPTER, MODEL # P/N 020-072-01 SELFCARE, INC.
K971777 05/14/1997 QUANTEX ASO-CRP-RF CONTROL INSTRUMENTATION LABORATORY CO.
K961991 05/21/1996 ACL 6000 SYSTEM (ACL 6000) INSTRUMENTATION LABORATORY CO.
K962198 06/07/1996 QUANTEX C4 INSTRUMENTATION LABORATORY CO.
K962199 06/07/1996 QUANTEX C3 INSTRUMENTATION LABORATORY CO.
K962200 06/07/1996 QUANTEX IGA INSTRUMENTATION LABORATORY CO.
K962201 06/07/1996 QUANTEX IGM INSTRUMENTATION LABORATORY CO.
K962202 06/07/1996 QUANTEX IGG INSTRUMENTATION LABORATORY CO.
K972363 06/25/1997 IL TEST IRON INSTRUMENTATION LABORATORY CO.
K972696 07/18/1997 IL TEST D-DIMER INSTRUMENTATION LABORATORY CO.
K972861 08/04/1997 IL TEST CONTRIL SPECTRUM (LEVELS 1, 2 AND 3) INSTRUMENTATION LABORATORY CO.
K963800 09/23/1996 IL SYNTHESIS INSTRUMENTATION LABORATORY CO.
K955793 12/22/1995 IL BGGE BLOOD GAS WITH GLUCOSE SYSTEM INSTRUMENTATION LABORATORY CO.


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