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ROTABLATOR ROTATIONAL ANGIOPLASTY SYSTEM ROTABLATOR SYSTEM'S GUIDE WIRE LINE; HTI FLOPPY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K954604
510(k) Type
Traditional
Applicant
HEART TECHNOLOGY MFG., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/1996
Days to Decision
106 days
Submission Type
Summary

ROTABLATOR ROTATIONAL ANGIOPLASTY SYSTEM ROTABLATOR SYSTEM'S GUIDE WIRE LINE; HTI FLOPPY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K954604
510(k) Type
Traditional
Applicant
HEART TECHNOLOGY MFG., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/1996
Days to Decision
106 days
Submission Type
Summary