510(k) K914171

IN VITRO DIAGNOSTIC REGEANT SET,CHOLINESTERASE by Tech Intl. Co. — Product Code DIH

K914171 is an FDA 510(k) premarket notification submitted by Tech Intl. Co. for the device "IN VITRO DIAGNOSTIC REGEANT SET,CHOLINESTERASE". The FDA issued a decision of Substantially Equivalent on December 18, 1991. The device falls under product code DIH (Colorimetry, Cholinesterase), a Class I device regulated under 21 CFR 862.3240. Tech Intl. Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 18, 1991
Date Received
September 17, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Colorimetry, Cholinesterase
Device Class
Class I
Regulation Number
862.3240
Review Panel
TX
Submission Type