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EDENTEC MODEL 2800/2801 OXIMETER/PULSE OXIMETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K881820
510(k) Type
Traditional
Applicant
EDENTEC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/1988
Days to Decision
80 days

EDENTEC MODEL 2800/2801 OXIMETER/PULSE OXIMETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K881820
510(k) Type
Traditional
Applicant
EDENTEC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/1988
Days to Decision
80 days