510(k) K000483

RANDOX ALBUMIN by Randox Laboratories, Ltd. — Product Code CJW

K000483 is an FDA 510(k) premarket notification submitted by Randox Laboratories, Ltd. for the device "RANDOX ALBUMIN". The FDA issued a decision of Substantially Equivalent on March 31, 2000. The device falls under product code CJW (Bromcresol Purple Dye-Binding, Albumin), a Class II device regulated under 21 CFR 862.1035. Randox Laboratories, Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 31, 2000
Date Received
February 14, 2000
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Bromcresol Purple Dye-Binding, Albumin
Device Class
Class II
Regulation Number
862.1035
Review Panel
CH
Submission Type