Intercare Diagnostics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Intercare Diagnostics, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Intercare Diagnostics, Inc. has 5 FDA 510(k) cleared medical devices. Based in Berkeley, US.
Historical record: 5 cleared submissions from 1986 to 1994. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Intercare Diagnostics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Intercare Diagnostics, Inc.
5 devices
Cleared
Aug 05, 1994
THE MIRAGE SYSTEM BIOFEEDBACK INTERFACE
Neurology
106d
Cleared
Feb 09, 1993
INDXTM DIP-S-TICKSTM
Microbiology
368d
Cleared
Dec 21, 1990
INDX DIP S TICKS
Microbiology
260d
Cleared
Jul 25, 1989
HEMATOLOGY CONTROL MIXTURES FOR QUALITY CONTROL
Hematology
56d
Cleared
Oct 17, 1986
CHLAMYDIA TISSUE CULTURE CONFIRMATION TEST (EIA)
Microbiology
73d