FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

RAPITEX(R) RF NEW

K Number: K903852 · Decision Aug 30, 1990
Classifications
1
FEI Numbers
59
Registration Numbers
59
Same Product Code
143
Applicant Total
145
Review Days
9

Basic Information

Device Name
RAPITEX(R) RF NEW
K Number
K903852
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5775
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
BEHRING DIAGNOSTICS, INC.
Date Received
August 21, 1990
Decision Date
August 30, 1990
Product Code
DHR
Advisory Committee
Immunology
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
DHR System, Test, Rheumatoid Factor

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