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SATLITE+/PB251+ PULSE OXIMETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K881883
510(k) Type
Traditional
Applicant
DATEX DIVISION INSTRUMENTARIUM CORP.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
7/18/1988
Days to Decision
75 days

SATLITE+/PB251+ PULSE OXIMETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K881883
510(k) Type
Traditional
Applicant
DATEX DIVISION INSTRUMENTARIUM CORP.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
7/18/1988
Days to Decision
75 days