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

UNIMETER 330K

K Number: K822441 · Decision Oct 8, 1982
Classifications
1
FEI Numbers
88
Registration Numbers
88
Same Product Code
87
Applicant Total
340
Review Days
53

Basic Information

Device Name
UNIMETER 330K
K Number
K822441
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1600
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
BOEHRINGER MANNHEIM CORP.
Date Received
August 16, 1982
Decision Date
October 8, 1982
Product Code
CEM
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
CEM Electrode, Ion Specific, Potassium

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