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AS/3 ANAESTHESIA MONITORING SYSTEM AIRWAY MODULE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K923433
510(k) Type
Traditional
Applicant
INSTRUMENTARIUM CORP.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
7/22/1993
Days to Decision
374 days
Submission Type
Statement

AS/3 ANAESTHESIA MONITORING SYSTEM AIRWAY MODULE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K923433
510(k) Type
Traditional
Applicant
INSTRUMENTARIUM CORP.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
7/22/1993
Days to Decision
374 days
Submission Type
Statement