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FDA 510(k) Applications Submitted by BETTY J LANE
FDA 510(k) Number
Submission Date
Device Name
Applicant
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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