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

ACA(R) DIGOXIN ANALYTICAL TEST PACK (DGN)

K Number: K932732 · Decision Nov 15, 1993
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
84
Applicant Total
28
Review Days
161

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Basic Information

Device Name
ACA(R) DIGOXIN ANALYTICAL TEST PACK (DGN)
K Number
K932732
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3320
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dupont Medical Products
Date Received
June 7, 1993
Decision Date
November 15, 1993
Product Code
KXT
Advisory Committee
Clinical Toxicology
Review Advisory Committee
TX
Third Party
N

Classifications

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

Product Code Device Name
KXT Enzyme Immunoassay, Digoxin

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