Kyoto Diagnostics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kyoto Diagnostics, Inc. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Kyoto Diagnostics, Inc. has 11 FDA 510(k) cleared chemistry devices. Based in Walker, US.
Historical record: 11 cleared submissions from 1984 to 1986.
Browse the complete list of FDA 510(k) cleared chemistry devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kyoto Diagnostics, Inc.
11 devices
Cleared
Jul 25, 1986
ADDITIONAL KYOTEST URINE TEST REAGENT STRIPS
Chemistry
80d
Cleared
Sep 28, 1984
GLUCOSE AUTO& STAT GA-1120
Toxicology
60d
Cleared
Aug 17, 1984
OSMOTIC PRESSURE AUTO & STAT OM-6010
Chemistry
35d
Cleared
Jul 16, 1984
ATAGO URINE SPECIFIC GRAVITY & SERUM
Chemistry
46d
Cleared
May 31, 1984
KYOTEST UG URINE TEST REAGENT STRIP
Chemistry
37d
Cleared
May 31, 1984
KYOTEST 2V, URINE TEST REAGENT STRIP
Chemistry
37d
Cleared
May 31, 1984
KYOTEST UK URINE TEST REAGENT STRIP
Chemistry
37d
Cleared
May 14, 1984
KYOTEST 5V
Chemistry
80d
Cleared
May 14, 1984
KYOTEST 8V
Hematology
80d
Cleared
May 01, 1984
URINE ANALYZER SYSTEM
Chemistry
54d
Cleared
Apr 19, 1984
KYOTEST UGK
Hematology
55d