Last synced on 20 December 2024 at 11:05 pm

ECHOHEART TRANSVAGINAL DOPPLER PROBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060410
510(k) Type
Traditional
Applicant
SUMMIT DOPPLER SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/2006
Days to Decision
53 days
Submission Type
Summary

ECHOHEART TRANSVAGINAL DOPPLER PROBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060410
510(k) Type
Traditional
Applicant
SUMMIT DOPPLER SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/2006
Days to Decision
53 days
Submission Type
Summary