Last synced on 23 May 2025 at 11:06 pm

MYOPERFUSION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K132523
510(k) Type
Traditional
Applicant
TOSHIBA MEDICAL SYSTEMS CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/12/2013
Days to Decision
122 days
Submission Type
Summary

MYOPERFUSION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K132523
510(k) Type
Traditional
Applicant
TOSHIBA MEDICAL SYSTEMS CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/12/2013
Days to Decision
122 days
Submission Type
Summary