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DOPPLEX CENTRALE

Page Type
Cleared 510(K)
510(k) Number
K060230
510(k) Type
Traditional
Applicant
HUNTLEIGH HEALTHCARE LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
3/23/2006
Days to Decision
52 days
Submission Type
Summary

DOPPLEX CENTRALE

Page Type
Cleared 510(K)
510(k) Number
K060230
510(k) Type
Traditional
Applicant
HUNTLEIGH HEALTHCARE LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
3/23/2006
Days to Decision
52 days
Submission Type
Summary