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ROTABLATOR SYSTEM'S GUIDE WIRE LINE: SUPPORT ROTAWIRE RAIL ROTA WIRE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960379
510(k) Type
Traditional
Applicant
HEART TECHNOLOGY MFG., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/25/1996
Days to Decision
90 days
Submission Type
Summary

ROTABLATOR SYSTEM'S GUIDE WIRE LINE: SUPPORT ROTAWIRE RAIL ROTA WIRE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960379
510(k) Type
Traditional
Applicant
HEART TECHNOLOGY MFG., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/25/1996
Days to Decision
90 days
Submission Type
Summary