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VESSEL DILATOR

Page Type
Cleared 510(K)
510(k) Number
K822595
510(k) Type
Traditional
Applicant
VERTEX MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/28/1982
Days to Decision
32 days

VESSEL DILATOR

Page Type
Cleared 510(K)
510(k) Number
K822595
510(k) Type
Traditional
Applicant
VERTEX MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/28/1982
Days to Decision
32 days