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DORO HEADREST SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K001808
510(k) Type
Traditional
Applicant
PRO-MED INSTRUMENTS GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/4/2000
Days to Decision
50 days
Submission Type
Summary

DORO HEADREST SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K001808
510(k) Type
Traditional
Applicant
PRO-MED INSTRUMENTS GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/4/2000
Days to Decision
50 days
Submission Type
Summary