Last synced on 19 July 2024 at 11:05 pm

MODIFICATION TO ONYX, FINGER CLIP PULSE OXIMETER, MODEL 9500

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001085
510(k) Type
Special
Applicant
NONIN MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/2000
Days to Decision
27 days
Submission Type
Summary

MODIFICATION TO ONYX, FINGER CLIP PULSE OXIMETER, MODEL 9500

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001085
510(k) Type
Special
Applicant
NONIN MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/2000
Days to Decision
27 days
Submission Type
Summary