510(k) K033983

VITALAB IRON REAGENT by Clinical Data, Inc. — Product Code JIY

K033983 is an FDA 510(k) premarket notification submitted by Clinical Data, Inc. for the device "VITALAB IRON REAGENT". The FDA issued a decision of Substantially Equivalent on May 21, 2004. The device falls under product code JIY (Photometric Method, Iron (Non-Heme)), a Class I device regulated under 21 CFR 862.1410. Clinical Data, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 21, 2004
Date Received
December 23, 2003
Clearance Type
Traditional
Expedited Review
No
Third Party Review
Yes

Device Classification

Device Name
Photometric Method, Iron (Non-Heme)
Device Class
Class I
Regulation Number
862.1410
Review Panel
CH
Submission Type