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PERIPHERAL ATHERECTOMY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K890515
510(k) Type
Traditional
Applicant
INTENSIVE TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/23/1989
Days to Decision
111 days

PERIPHERAL ATHERECTOMY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K890515
510(k) Type
Traditional
Applicant
INTENSIVE TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/23/1989
Days to Decision
111 days