Last synced on 23 May 2025 at 11:06 pm

INFX-8000C (INFINIX CC-I AND VC-I)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081621
510(k) Type
Traditional
Applicant
TOSHIBA AMERICA MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/23/2008
Days to Decision
14 days
Submission Type
Summary

INFX-8000C (INFINIX CC-I AND VC-I)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081621
510(k) Type
Traditional
Applicant
TOSHIBA AMERICA MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/23/2008
Days to Decision
14 days
Submission Type
Summary