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0.016 GUIDE WIRE FOR NEUROLOGICAL ENDOSCOPE

Page Type
Cleared 510(K)
510(k) Number
K913074
510(k) Type
Traditional
Applicant
TERUMO MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/1991
Days to Decision
117 days
Submission Type
Statement

0.016 GUIDE WIRE FOR NEUROLOGICAL ENDOSCOPE

Page Type
Cleared 510(K)
510(k) Number
K913074
510(k) Type
Traditional
Applicant
TERUMO MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/1991
Days to Decision
117 days
Submission Type
Statement