510(k) K942501

ACE CEDIA PHENOBARBITAL ASSAY by Schiapparelli Biosystems, Inc. — Product Code DLZ

K942501 is an FDA 510(k) premarket notification submitted by Schiapparelli Biosystems, Inc. for the device "ACE CEDIA PHENOBARBITAL ASSAY". The FDA issued a decision of Substantially Equivalent on October 6, 1994. The device falls under product code DLZ (Enzyme Immunoassay, Phenobarbital), a Class II device regulated under 21 CFR 862.3660. Schiapparelli Biosystems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 6, 1994
Date Received
May 24, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Enzyme Immunoassay, Phenobarbital
Device Class
Class II
Regulation Number
862.3660
Review Panel
TX
Submission Type