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ANASTOMART(TM) CORONARY BYPASS GRAFT MARKERS/MODIF

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K922025
510(k) Type
Traditional
Applicant
PIONEERING TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/22/1992
Days to Decision
168 days
Submission Type
Statement

ANASTOMART(TM) CORONARY BYPASS GRAFT MARKERS/MODIF

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K922025
510(k) Type
Traditional
Applicant
PIONEERING TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/22/1992
Days to Decision
168 days
Submission Type
Statement