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VESSEL DILATOR

Page Type
Cleared 510(K)
510(k) Number
K963388
510(k) Type
Traditional
Applicant
MAXXIM MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/1997
Days to Decision
195 days
Submission Type
Summary

VESSEL DILATOR

Page Type
Cleared 510(K)
510(k) Number
K963388
510(k) Type
Traditional
Applicant
MAXXIM MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/1997
Days to Decision
195 days
Submission Type
Summary