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PERCUSSIVETECH HF, MODEL 2001

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981726
510(k) Type
Traditional
Applicant
VORTRAN MEDICAL TECHNOLOGY 1, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/1998
Days to Decision
125 days
Submission Type
Statement

PERCUSSIVETECH HF, MODEL 2001

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981726
510(k) Type
Traditional
Applicant
VORTRAN MEDICAL TECHNOLOGY 1, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/1998
Days to Decision
125 days
Submission Type
Statement