510(k) K946143

CHEMSPEX(TM) AMMONIA CONTROL by Clinical Controls, Inc. — Product Code JJX

K946143 is an FDA 510(k) premarket notification submitted by Clinical Controls, Inc. for the device "CHEMSPEX(TM) AMMONIA CONTROL". The FDA issued a decision of Substantially Equivalent on February 3, 1995. The device falls under product code JJX (Single (Specified) Analyte Controls (Assayed And Unassayed)), a Class I device regulated under 21 CFR 862.1660. Clinical Controls, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 3, 1995
Date Received
December 16, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Single (Specified) Analyte Controls (Assayed And Unassayed)
Device Class
Class I
Regulation Number
862.1660
Review Panel
CH
Submission Type