Last synced on 19 July 2024 at 11:05 pm

XENOVIEW 3.0T Chest Coil

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212239
510(k) Type
Traditional
Applicant
Polarean, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/23/2022
Days to Decision
522 days
Submission Type
Summary

XENOVIEW 3.0T Chest Coil

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212239
510(k) Type
Traditional
Applicant
Polarean, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/23/2022
Days to Decision
522 days
Submission Type
Summary