Disease Detection International, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Disease Detection International, Inc. - FDA 510(k) Cleared Devices
20
Total
20
Cleared
0
Denied
Disease Detection International, Inc. has 20 FDA 510(k) cleared medical devices. Based in Irvine, US.
Historical record: 20 cleared submissions from 1988 to 1994. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Disease Detection International, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Disease Detection International, Inc.
20 devices
Cleared
Oct 25, 1994
PRO-STEP LH OVULATION PREDICTION TEST
Chemistry
111d
Cleared
Jun 15, 1993
PRO-STEP PT HCG
Chemistry
237d
Cleared
Jan 13, 1993
PRO-STEP HCG
Chemistry
92d
Cleared
Jul 19, 1991
IMMUNOCARD HCG ONE STEP (I-S) TEST KIT
Chemistry
86d
Cleared
Sep 05, 1990
MODIFICATION OF SEROCARD RUBELLA IGG TEST
Microbiology
90d
Cleared
Aug 09, 1990
SEROCARD HSV IGG ANTIBODY TEST KIT
Microbiology
28d
Cleared
Dec 01, 1989
IMMUNOCARD HCG II-S TEST KIT
Chemistry
52d
Cleared
Nov 29, 1989
IMMUNOCARD STREP A TEST
Microbiology
37d
Cleared
Apr 10, 1989
MODIFIED DDI SEROCARD HERPES IGG TEST KIT
Microbiology
181d
Cleared
Apr 10, 1989
MODIFIED DDI SEROCARD RUBELLA IGG TEST KIT
Microbiology
181d
Cleared
Apr 10, 1989
MODIFIED DDI SEROCARD CMV IGG TEST KIT
Microbiology
181d
Cleared
Apr 10, 1989
MODIFIED DDI SEROCARD TOXOPLASMA IGG TEST KIT
Microbiology
181d