FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ACE(TM) CEDIA(R) PHENYTOIN ASSAY

K Number: K944085 · Decision Dec 28, 1994
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
43
Applicant Total
24
Review Days
128

Basic Information

Device Name
ACE(TM) CEDIA(R) PHENYTOIN ASSAY
K Number
K944085
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3350
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SCHIAPPARELLI BIOSYSTEMS, INC.
Date Received
August 22, 1994
Decision Date
December 28, 1994
Product Code
DIP
Advisory Committee
Clinical Toxicology
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DIP Enzyme Immunoassay, Diphenylhydantoin

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Other Clearances by SCHIAPPARELLI BIOSYSTEMS, INC.

K Number Device Name
K991733 ACE LDL-C REAGENT, LDL-C CALIBRATOR, LDL-C CONTROLS
K981377 ACE T4 REAGENT T4 CALIBRATORS
K981375 ACE T UPTAKE REAGENT TU CALIBRATORS
K973581 ACE VALPROIC ACID REAGENT, AED CALIBRATORS
K973582 ACE PRIMIDONE REAGENT, AED CALIBRATORS
K973583 ACE THEOPHYLLINE REAGENT, THEO CALIBRATORS
K973536 ACE PHENOBARBITAL REAGENT/AED CALIBRATORS
K973414 ACE PHENYTOIN REAGENT, AED CALIBRATORS
K973535 ACE CARBAMAZEPINE REAGENT/AED CALIBRATORS
K971526 ACE HDL-C REAGENT
Search all 24 clearances from SCHIAPPARELLI BIOSYSTEMS, INC. →