Last synced on 14 November 2025 at 11:06 pm

M-PATH NITINOL GUIDEWIRE

Page Type
Cleared 510(K)
510(k) Number
K946356
510(k) Type
Traditional
Applicant
MICROVENA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/1995
Days to Decision
91 days
Submission Type
Statement

M-PATH NITINOL GUIDEWIRE

Page Type
Cleared 510(K)
510(k) Number
K946356
510(k) Type
Traditional
Applicant
MICROVENA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/1995
Days to Decision
91 days
Submission Type
Statement