Last synced on 29 September 2023 at 11:04 pm

MODIFICATION TO HIOX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030943
510(k) Type
Traditional
Applicant
SENSOR MEDICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/22/2003
Days to Decision
27 days
Submission Type
Summary

MODIFICATION TO HIOX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030943
510(k) Type
Traditional
Applicant
SENSOR MEDICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/22/2003
Days to Decision
27 days
Submission Type
Summary