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CRITIKON OXYGEN MONITOR, MODEL 8030

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K821936
510(k) Type
Traditional
Applicant
CRITIKON COMPANY,LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/1982
Days to Decision
48 days

CRITIKON OXYGEN MONITOR, MODEL 8030

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K821936
510(k) Type
Traditional
Applicant
CRITIKON COMPANY,LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/1982
Days to Decision
48 days