510(k) K936202

URINARY ALBUMIN TEST PACK by Dupont Medical Products — Product Code JIQ

K936202 is an FDA 510(k) premarket notification submitted by Dupont Medical Products for the device "URINARY ALBUMIN TEST PACK". The FDA issued a decision of Substantially Equivalent on May 9, 1994. The device falls under product code JIQ (Turbidimetric Method, Protein Or Albumin (Urinary, Non-Quant.)), a Class I device regulated under 21 CFR 862.1645. Dupont Medical Products has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 9, 1994
Date Received
December 29, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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