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VERTEX MONITORING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K823253
510(k) Type
Traditional
Applicant
VERTEX MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/30/1982
Days to Decision
59 days

VERTEX MONITORING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K823253
510(k) Type
Traditional
Applicant
VERTEX MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/30/1982
Days to Decision
59 days