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

MODIFICATION OF BEHRING RAPIMAT II/T

K Number: K882095 · Decision Aug 2, 1988
Classifications
1
FEI Numbers
85
Registration Numbers
85
Same Product Code
257
Applicant Total
145
Review Days
75

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Basic Information

Device Name
MODIFICATION OF BEHRING RAPIMAT II/T
K Number
K882095
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2300
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Behring Diagnostics, Inc.
Date Received
May 19, 1988
Decision Date
August 2, 1988
Product Code
JJQ
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
JJQ Colorimeter, Photometer, Spectrophotometer For Clinical Use

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