Last synced on 25 January 2026 at 3:41 am

OXIBLUE FINGERTIP PULSE OXIMETER MODEL MD300C318, OXIPRO FINGERTIP PULSE OXIMETER MODEL MD300C316

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100815
510(k) Type
Traditional
Applicant
Oxypulse
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/16/2010
Days to Decision
85 days
Submission Type
Statement

OXIBLUE FINGERTIP PULSE OXIMETER MODEL MD300C318, OXIPRO FINGERTIP PULSE OXIMETER MODEL MD300C316

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100815
510(k) Type
Traditional
Applicant
Oxypulse
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/16/2010
Days to Decision
85 days
Submission Type
Statement