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

ARCHITECT TOTAL P-HCG MASTERCHECK, LIST NO. 6C21-05

K Number: K984073 · Decision Nov 25, 1998
Classifications
1
FEI Numbers
280
Registration Numbers
280
Same Product Code
492
Applicant Total
318
Review Days
9

Basic Information

Device Name
ARCHITECT TOTAL P-HCG MASTERCHECK, LIST NO. 6C21-05
K Number
K984073
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
BIO-RAD
Date Received
November 16, 1998
Decision Date
November 25, 1998
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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