510(k) K894169

BIOTEL MICROALBUMINURIA (TM) by American Diagnostic Corp. — Product Code JIR

K894169 is an FDA 510(k) premarket notification submitted by American Diagnostic Corp. for the device "BIOTEL MICROALBUMINURIA (TM)". The FDA issued a decision of Substantially Equivalent on September 18, 1989. 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 Diagnostic Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 18, 1989
Date Received
June 15, 1989
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