Immunoprobe, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Immunoprobe, Inc. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Immunoprobe, Inc. has 14 FDA 510(k) cleared immunology devices. Based in Washington, US.
Historical record: 14 cleared submissions from 1994 to 1997.
Browse the complete list of FDA 510(k) cleared immunology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Immunoprobe, Inc.
14 devices
Cleared
Dec 22, 1997
ADENOVIRUS ANTIGEN DETECTION ELISA TEST SYSTEM
Microbiology
179d
Cleared
Jul 14, 1997
MYCOPLASMA IGG ELISA TEST SYSTEM
Microbiology
96d
Cleared
Aug 19, 1996
PR-3 ELISA TEST SYSTEM
Immunology
104d
Cleared
Aug 19, 1996
MPO ELISA TEST SYSTEM
Immunology
104d
Cleared
Apr 29, 1996
EBNA IGG EIA TEST SYSTEM
Microbiology
391d
Cleared
Feb 09, 1996
CARDIOLIPIN IGM EIA TEST SYSTEM
Immunology
253d
Cleared
Feb 09, 1996
CARDIOLIPIN IGA EIA TEST SYSTEM
Immunology
253d
Cleared
Feb 09, 1996
CARDIOLIPIN IGG EIA TEST KIT
Immunology
253d
Cleared
Nov 20, 1995
THYROGLOBULIN EIA TEST KIT
Immunology
241d
Cleared
Nov 20, 1995
MICROSOMAL EIA TEST KIT
Immunology
241d
Cleared
Oct 13, 1995
CARDIOLIPIN IGG,M,A EIA TEST SYSTEM
Immunology
203d
Cleared
Sep 15, 1995
CARDIOLIPIN IGG,M,A EIA TEST KIT
Immunology
106d
Cleared
May 11, 1994
THYROGLOBULIN EIA TEST KIT
Immunology
51d
Cleared
May 11, 1994
MICROSOMAL EIA TEST KIT
Immunology
51d