Last synced on 19 July 2024 at 11:05 pm

OxyMinder

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213948
510(k) Type
Traditional
Applicant
Bio-Med Devices, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/17/2022
Days to Decision
90 days
Submission Type
Summary

OxyMinder

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213948
510(k) Type
Traditional
Applicant
Bio-Med Devices, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/17/2022
Days to Decision
90 days
Submission Type
Summary