Immuno Diagnostic Center, Inc.
Country not established FDA establishment FEI 1000118715
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
What Immuno Diagnostic Center, Inc. makes
IMMUNO DIAGNOSTIC CENTER, INC. manufactures in vitro diagnostic test kits, including the MICRO ALBUMIN EIA TEST KIT, MYOGLOBIN ELISA TEST KIT, and MYOGLOBIN RIA TEST KIT.
The company's products are regulated as Class I and Class II devices and are listed in the FDA 510(k) registry. IMMUNO DIAGNOSTIC CENTER, INC. is based in the US.
Catalogue
Micro Albumin Eia Test Kit Ref K912543
510(k) 510(k)Myoglobin Elisa Test Kit Ref K923195
510(k) 510(k)Myoglobin Ria Test Kit Ref K904038
510(k) 510(k)
Company details
- FDA FEI number
- 1000118715
- Address
- 10042 MONROE DRIVE, DALLAS, TX, 75229
Frequently asked questions
How many devices does IMMUNO DIAGNOSTIC CENTER, INC. have in the registry?
The registry currently lists 3 devices for IMMUNO DIAGNOSTIC CENTER, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list IMMUNO DIAGNOSTIC CENTER, INC.'s devices?
Among its 3 most recently registered devices, IMMUNO DIAGNOSTIC CENTER, INC. has devices listed in FDA 510(k) (3 devices).
What risk classes do IMMUNO DIAGNOSTIC CENTER, INC.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for IMMUNO DIAGNOSTIC CENTER, INC.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from IMMUNO DIAGNOSTIC CENTER, INC. in the registry?
The most recently registered devices listed for IMMUNO DIAGNOSTIC CENTER, INC. include MICRO ALBUMIN EIA TEST KIT, MYOGLOBIN ELISA TEST KIT and MYOGLOBIN RIA TEST KIT.