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OXITRON OXYGEN ANALYZER

Page Type
Cleared 510(K)
510(k) Number
K890958
510(k) Type
Traditional
Applicant
OXITRON MEDICAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/22/1989
Days to Decision
84 days

OXITRON OXYGEN ANALYZER

Page Type
Cleared 510(K)
510(k) Number
K890958
510(k) Type
Traditional
Applicant
OXITRON MEDICAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/22/1989
Days to Decision
84 days