Last synced on 20 December 2024 at 11:05 pm

8ch Wrist Coil

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222325
510(k) Type
Traditional
Applicant
Invivo Corporation (Business Trade Name: Philips)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/31/2022
Days to Decision
29 days
Submission Type
Summary

8ch Wrist Coil

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222325
510(k) Type
Traditional
Applicant
Invivo Corporation (Business Trade Name: Philips)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/31/2022
Days to Decision
29 days
Submission Type
Summary