510(k) K970932

ORGENTEC MICRO-ALBUMIN EIA ASSAY by American Laboratory Products Co., Ltd. — Product Code JIR

K970932 is an FDA 510(k) premarket notification submitted by American Laboratory Products Co., Ltd. for the device "ORGENTEC MICRO-ALBUMIN EIA ASSAY". The FDA issued a decision of Substantially Equivalent on April 8, 1997. 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. American Laboratory Products Co., Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 8, 1997
Date Received
February 20, 1997
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