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CERION HAND HELD OXYGEN ANALYZER

Page Type
Cleared 510(K)
510(k) Number
K911344
510(k) Type
Traditional
Applicant
CERAMATEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/18/1991
Days to Decision
83 days

CERION HAND HELD OXYGEN ANALYZER

Page Type
Cleared 510(K)
510(k) Number
K911344
510(k) Type
Traditional
Applicant
CERAMATEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/18/1991
Days to Decision
83 days