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DORO RADIOLUCENT HEADREST SYSTEM ( ALSO MRI-COMPATIBLE) AND COMPONENTS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063494
510(k) Type
Traditional
Applicant
PRO-MED INSTRUMENTS GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/21/2007
Days to Decision
182 days
Submission Type
Summary

DORO RADIOLUCENT HEADREST SYSTEM ( ALSO MRI-COMPATIBLE) AND COMPONENTS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063494
510(k) Type
Traditional
Applicant
PRO-MED INSTRUMENTS GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/21/2007
Days to Decision
182 days
Submission Type
Summary