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ONYX II FINGER PULSE OXIMETER, MODEL 9550

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K053130
510(k) Type
Traditional
Applicant
Nonin Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/11/2006
Days to Decision
64 days
Submission Type
Summary

ONYX II FINGER PULSE OXIMETER, MODEL 9550

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K053130
510(k) Type
Traditional
Applicant
Nonin Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/11/2006
Days to Decision
64 days
Submission Type
Summary