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SURGITEK(R) 420 CM G.I. INFUSION GUIDEWIRE

Page Type
Cleared 510(K)
510(k) Number
K910768
510(k) Type
Traditional
Applicant
SURGITEK MEDICAL ENGINEERING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/19/1991
Days to Decision
25 days

SURGITEK(R) 420 CM G.I. INFUSION GUIDEWIRE

Page Type
Cleared 510(K)
510(k) Number
K910768
510(k) Type
Traditional
Applicant
SURGITEK MEDICAL ENGINEERING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/19/1991
Days to Decision
25 days