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

ABBOTT HCG SERUM CONTROLS

K Number: K970527 · Decision Mar 3, 1997
Classifications
1
FEI Numbers
280
Registration Numbers
280
Same Product Code
492
Applicant Total
857
Review Days
20

Basic Information

Device Name
ABBOTT HCG SERUM CONTROLS
K Number
K970527
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ABBOTT LABORATORIES
Date Received
February 11, 1997
Decision Date
March 3, 1997
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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