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PERCUSSIVETECH HF, MODEL 2001

Page Type
Cleared 510(K)
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)
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