510(k) K855239

BIOTEL (TM)/ DIABETES by American Diagnostic Corp. — Product Code JIL

K855239 is an FDA 510(k) premarket notification submitted by American Diagnostic Corp. for the device "BIOTEL (TM)/ DIABETES". The FDA issued a decision of Substantially Equivalent on June 13, 1986. The device falls under product code JIL (Method, Enzymatic, Glucose (Urinary, Non-Quantitative)), a Class II device regulated under 21 CFR 862.1340. American Diagnostic Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 13, 1986
Date Received
December 31, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Method, Enzymatic, Glucose (Urinary, Non-Quantitative)
Device Class
Class II
Regulation Number
862.1340
Review Panel
CH
Submission Type