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

ROCHE CONTROL SERUM P

K Number: K954656 · Decision Dec 21, 1995
Classifications
1
FEI Numbers
135
Registration Numbers
135
Same Product Code
672
Applicant Total
296
Review Days
72

Basic Information

Device Name
ROCHE CONTROL SERUM P
K Number
K954656
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
ROCHE DIAGNOSTIC SYSTEMS, INC.
Date Received
October 10, 1995
Decision Date
December 21, 1995
Product Code
JJY
Advisory Committee
Clinical Chemistry
Review Advisory Committee
IM
Third Party
N

Classifications

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

Product Code Device Name
JJY Multi-Analyte Controls, All Kinds (Assayed)

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