In Vitro Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
In Vitro Technologies, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
In Vitro Technologies, Inc. has 7 FDA 510(k) cleared medical devices. Based in Arlington, US.
Historical record: 7 cleared submissions from 1987 to 1992. Primary specialty: Immunology.
Browse the FDA 510(k) cleared devices submitted by In Vitro Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - In Vitro Technologies, Inc.
7 devices
Cleared
Sep 14, 1992
866.5750 RADIOALLERGOSORBENT IMMUNLOGICAL TEST SYS
Immunology
332d
Cleared
Nov 29, 1990
IVT RAST TRACER
Immunology
48d
Cleared
Apr 07, 1988
IVT CENTRAL ALLERGY SCREEN
Immunology
99d
Cleared
Mar 23, 1988
IVT WESTERN ALLERGY SCREEN
Immunology
84d
Cleared
Jan 11, 1988
IVT SOUTHEAST ALLERGY SCREEN
Immunology
90d
Cleared
Jan 11, 1988
IVT NORTHEAST ALLERGY SCREEN
Immunology
90d
Cleared
May 01, 1987
IVT SOUTHWEST ALLERGY SCREEN
Immunology
77d