510(k) K994035

IMMUNODIP URINARY ALBUMIN SCREEN, MODEL 790-01, 790-15 by Diagnostic Chemicals , Ltd. — Product Code JIR

K994035 is an FDA 510(k) premarket notification submitted by Diagnostic Chemicals , Ltd. for the device "IMMUNODIP URINARY ALBUMIN SCREEN, MODEL 790-01, 790-15". The FDA issued a decision of Substantially Equivalent on February 1, 2000. The device falls under product code JIR (Indicator Method, Protein Or Albumin (Urinary, Non-Quant.)), a Class I device regulated under 21 CFR 862.1645. Diagnostic Chemicals , Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 1, 2000
Date Received
November 29, 1999
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Indicator Method, Protein Or Albumin (Urinary, Non-Quant.)
Device Class
Class I
Regulation Number
862.1645
Review Panel
CH
Submission Type