Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K960412
Device Classification Name
Radioimmunoassay, Total Triiodothyronine
More FDA Info for this Device
510(K) Number
K960412
Device Name
Radioimmunoassay, Total Triiodothyronine
Applicant
BIOMERICA, INC.
1533 MONROVIA AVE.
NEWPORT BEACH, CA 92663 US
Other 510(k) Applications for this Company
Contact
JOSEPH IRANI
Other 510(k) Applications for this Contact
Regulation Number
862.1710
More FDA Info for this Regulation Number
Classification Product Code
CDP
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
01/29/1996
Decision Date
03/19/1996
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CH - Clinical Chemistry
Review Advisory Committee
CH - Clinical Chemistry
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact