Miles, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Miles, Inc. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Miles, Inc. has 11 FDA 510(k) cleared chemistry devices. Based in Tarrytown, US.
Historical record: 11 cleared submissions from 1993 to 1995.
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 - Miles, Inc.
11 devices
Cleared
May 02, 1995
FOLATE ASSAY FOR THE TECHNICON IMMUNO 1 SYSTEM, IN VITRO DIAGNOSTIC SYSTEM
Chemistry
97d
Cleared
Apr 20, 1995
TECHNICON IMMUNO 1(R) SYSTEM IN-VITRO DIAGNOSTIC SYSTEM
Chemistry
80d
Cleared
Mar 13, 1995
CK-MB METHOD FOR THE TECHNICON IMMUNO 1(R) SYSTEM IN-VITRO DIAGNOSTIC SYSTEM
Chemistry
55d
Cleared
Jan 05, 1995
CREATININE (ENZYMATIC UV) PROCEDURE FOR TECHNICON SYSTEMS (IN VITRO...
Chemistry
49d
Cleared
Dec 14, 1994
TECHNICON H* 3 RTC SYSTEM (IN-VITRO DIAGNOSTIC SYSTEM)
Hematology
275d
Cleared
Sep 14, 1994
OPERA SYSTEM
Chemistry
63d
Cleared
Apr 26, 1994
TECHNISON AXON SYSTEM
Chemistry
47d
Cleared
Apr 12, 1994
DIRECT AMYLASE (EC 3.2.1.1) METHOD FOR TECHNICON SYSTEMS
Chemistry
257d
Cleared
Jan 03, 1994
IRON -II (FE-II) METHOD/TECH CHEM 1(R) 1+TM SYSTEM
Chemistry
61d
Cleared
Nov 22, 1993
TECHNICON H* 2 SYSTEM, LABFACTS SOFTWARE FOR U.I.W. VERSIONS 4.11 & 5.11
Hematology
129d
Cleared
Nov 22, 1993
TECHNICON H*1 SYSTEMS, LABFACTS SOFTWARE FOR U.I.W. VERSIONS 4.11 & 5.11
Hematology
129d