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

VISTA INSTRUMENT

K Number: K882914 · Decision Aug 30, 1988
Classifications
1
FEI Numbers
180
Registration Numbers
180
Same Product Code
207
Applicant Total
857
Review Days
49

Basic Information

Device Name
VISTA INSTRUMENT
K Number
K882914
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2160
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
ABBOTT LABORATORIES
Date Received
July 12, 1988
Decision Date
August 30, 1988
Product Code
JJE
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
JJE Analyzer, Chemistry (Photometric, Discrete), For Clinical Use

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