Ortho Diagnostics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ortho Diagnostics, Inc. - FDA 510(k) Cleared Devices
24
Total
24
Cleared
0
Denied
Ortho Diagnostics, Inc. has 24 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 24 cleared submissions from 1977 to 1980. Primary specialty: Hematology.
Browse the FDA 510(k) cleared devices submitted by Ortho Diagnostics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ortho Diagnostics, Inc.
24 devices
Cleared
Oct 23, 1980
ORTHO BOVINE ALBUMIN SOLUTION 30% PROTE
Immunology
17d
Cleared
Aug 20, 1980
ANTIGEN CONTROL CELLS
Microbiology
51d
Cleared
Apr 16, 1980
BI-LEVEL ASSAYED CARD. DRUG CONT., I,II
Toxicology
56d
Cleared
Mar 05, 1980
ORTHO ANTISERA CONTROL
Hematology
22d
Cleared
Oct 11, 1979
ORTHO ANTIBODY ENHANCEMENT SOLUTION
Hematology
30d
Cleared
Sep 24, 1979
ORTHO TSH RIA KIT
Chemistry
70d
Cleared
Jun 28, 1979
MULTECON BLOOD GAS CONTROL
Chemistry
62d
Cleared
Apr 04, 1979
PREGNANCY, SENSIDEX TUBE TEST
Chemistry
114d
Cleared
Apr 04, 1979
SLIDE TEST FOR PREGNANCY, GRAVINDEX 90
Chemistry
96d
Cleared
Dec 20, 1978
RUBINDEX*DIRECT SYSTEM
Immunology
90d
Cleared
Dec 04, 1978
ASSAY, CHROMOGENIC ANTITHROMBIN III
Chemistry
28d
Cleared
Oct 17, 1978
NORMAL HEMATOLOGY CONTROL UNASSAYED
Hematology
33d