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SURGITEK PERCUTANEOUS ARNEGRADE SILITEK

Page Type
Cleared 510(K)
510(k) Number
K831857
510(k) Type
Traditional
Applicant
MEDICAL ENGINEERING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/11/1983
Days to Decision
63 days

SURGITEK PERCUTANEOUS ARNEGRADE SILITEK

Page Type
Cleared 510(K)
510(k) Number
K831857
510(k) Type
Traditional
Applicant
MEDICAL ENGINEERING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/11/1983
Days to Decision
63 days