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KAMAR ANNULUS DILATOR + SIZER; GARRETT, COOLEY, AND DEBAKEY VESSEL DILATORS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030788
510(k) Type
Traditional
Applicant
GEISTER MEDIZINTECHNIK GMBH
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
7/12/2003
Days to Decision
122 days
Submission Type
Statement

KAMAR ANNULUS DILATOR + SIZER; GARRETT, COOLEY, AND DEBAKEY VESSEL DILATORS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030788
510(k) Type
Traditional
Applicant
GEISTER MEDIZINTECHNIK GMBH
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
7/12/2003
Days to Decision
122 days
Submission Type
Statement