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OXITRON OXYGEN ANALYZER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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