Last synced on 21 June 2024 at 11:04 pm

DORO LUCENT® iXI and iMRI Headrest System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K191740
510(k) Type
Traditional
Applicant
Pro Med Instruments GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
2/21/2020
Days to Decision
235 days
Submission Type
Summary

DORO LUCENT® iXI and iMRI Headrest System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K191740
510(k) Type
Traditional
Applicant
Pro Med Instruments GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
2/21/2020
Days to Decision
235 days
Submission Type
Summary