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

COBAS CORE PROLACTIN EIA

K Number: K930305 · Decision Aug 19, 1993
Classifications
1
FEI Numbers
58
Registration Numbers
58
Same Product Code
79
Applicant Total
296
Review Days
210

Basic Information

Device Name
COBAS CORE PROLACTIN EIA
K Number
K930305
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1625
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
ROCHE DIAGNOSTIC SYSTEMS, INC.
Date Received
January 21, 1993
Decision Date
August 19, 1993
Product Code
CFT
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
CFT Radioimmunoassay, Prolactin (Lactogen)

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