Last synced on 20 December 2024 at 11:05 pm

TEM 3000 HEAD COIL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052200
510(k) Type
Traditional
Applicant
MR INSTRUMENTS INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/19/2005
Days to Decision
7 days
Submission Type
Summary

TEM 3000 HEAD COIL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052200
510(k) Type
Traditional
Applicant
MR INSTRUMENTS INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/19/2005
Days to Decision
7 days
Submission Type
Summary