FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

OPUS HCG CONTROLS

K Number: K954144 · Decision Oct 6, 1995
Classifications
1
FEI Numbers
280
Registration Numbers
280
Same Product Code
492
Applicant Total
145
Review Days
31

Basic Information

Device Name
OPUS HCG CONTROLS
K Number
K954144
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
BEHRING DIAGNOSTICS, INC.
Date Received
September 5, 1995
Decision Date
October 6, 1995
Product Code
JJX
Advisory Committee
Clinical Chemistry
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
JJX Single (Specified) Analyte Controls (Assayed And Unassayed)

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