Diagnostic Systems Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Diagnostic Systems Laboratories, Inc. - FDA 510(k) Cleared Devices
94
Total
94
Cleared
0
Denied
Diagnostic Systems Laboratories, Inc. has 94 FDA 510(k) cleared chemistry devices. Based in Mchenry, US.
Historical record: 94 cleared submissions from 1981 to 2006.
Browse the complete list of FDA 510(k) cleared chemistry devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Diagnostic Systems Laboratories, Inc.
94 devices
Cleared
Jul 28, 2006
ACTIVE RENIN IRMA
Chemistry
36d
Cleared
May 31, 2002
AXSYM INTACT PTH, MODEL 2G06
Chemistry
67d
Cleared
Mar 01, 2002
ACTIVE FREE BETA-HCG ELISA, MODEL DSL-10-8500
Chemistry
45d
Cleared
Dec 05, 2000
ACTIVE INHIBIN-A ELISA, MODEL DSL-10-28100
Chemistry
144d
Cleared
May 18, 2000
FREE TESTOSTERONE ENZYME IMMUNOASSAY, MODEL DSL-10-4900
Immunology
44d
Cleared
Jun 21, 1999
DSL ACTIVE AFP ELISA, MODEL DSL-10-8400
Immunology
153d
Cleared
Nov 09, 1998
C-REACTIVE PROTEIN ELISA, MODEL NUMBER DSL-10-42100
Immunology
165d
Cleared
Aug 03, 1998
ACTIVE PSA ELISA (DSL-10-9700)
Immunology
339d
Cleared
Aug 03, 1998
ACTIVE PSA IRMA (DSL-9700)
Immunology
339d
Cleared
May 27, 1998
ACTIVE RENIN IRMA MODEL NUMBER DSL-25100
Chemistry
22d
Cleared
Oct 31, 1997
ACTIVE INTACT PTH
Chemistry
44d
Cleared
Jun 16, 1997
ACTIVE TESTOSTERONE EIA (DSL-10-4000)
Chemistry
31d
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