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GUIDANT VASOVIEW HEMOPRO ENDOSCOPIC VESSEL HARVESTING SYSTEM, MODEL VH-3000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052274
510(k) Type
Special
Applicant
GUIDANT CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/2005
Days to Decision
30 days
Submission Type
Summary

GUIDANT VASOVIEW HEMOPRO ENDOSCOPIC VESSEL HARVESTING SYSTEM, MODEL VH-3000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052274
510(k) Type
Special
Applicant
GUIDANT CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/2005
Days to Decision
30 days
Submission Type
Summary