Last synced on 14 November 2025 at 11:06 pm

XENOVIEW 3.0T Chest Coil

Page Type
Cleared 510(K)
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)
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