510(k) K000781

DIRECT TIBC KIT by Reference Diagnostics, Inc. — Product Code JMO

K000781 is an FDA 510(k) premarket notification submitted by Reference Diagnostics, Inc. for the device "DIRECT TIBC KIT". The FDA issued a decision of Substantially Equivalent on May 2, 2000. The device falls under product code JMO (Ferrozine (Colorimetric) Iron Binding Capacity), a Class I device regulated under 21 CFR 862.1415. Reference Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 2, 2000
Date Received
March 10, 2000
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Ferrozine (Colorimetric) Iron Binding Capacity
Device Class
Class I
Regulation Number
862.1415
Review Panel
CH
Submission Type