Last synced on 14 November 2025 at 11:06 pm

dS Sentinelle Breast 16ch 3.0T Coil

Page Type
Cleared 510(K)
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)
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