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VASCOSCREW 6/60 AND VASCOSCREW 8/60

Page Type
Cleared 510(K)
510(k) Number
K914121
510(k) Type
Traditional
Applicant
VASCOR MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/1993
Days to Decision
711 days
Submission Type
Summary

VASCOSCREW 6/60 AND VASCOSCREW 8/60

Page Type
Cleared 510(K)
510(k) Number
K914121
510(k) Type
Traditional
Applicant
VASCOR MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/1993
Days to Decision
711 days
Submission Type
Summary