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CRITIKON OXYGEN MONITOR, MODEL 8030

Page Type
Cleared 510(K)
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)
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