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DORO QR3 XTom Headholder System

Page Type
Cleared 510(K)
510(k) Number
K191979
510(k) Type
Traditional
Applicant
Pro Med Instruments GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
10/22/2019
Days to Decision
90 days
Submission Type
Summary

DORO QR3 XTom Headholder System

Page Type
Cleared 510(K)
510(k) Number
K191979
510(k) Type
Traditional
Applicant
Pro Med Instruments GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
10/22/2019
Days to Decision
90 days
Submission Type
Summary