Last synced on 5 July 2024 at 11:05 pm

dS Sentinelle Breast 16ch 3.0T Coil

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213727
510(k) Type
Traditional
Applicant
Invivo Corporation (Business Trade Name: Philips)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/2022
Days to Decision
255 days
Submission Type
Summary

dS Sentinelle Breast 16ch 3.0T Coil

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213727
510(k) Type
Traditional
Applicant
Invivo Corporation (Business Trade Name: Philips)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/2022
Days to Decision
255 days
Submission Type
Summary