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ULTRA-ASEPT ANGIOGRAPHIC SYRINGE/SPARE

Page Type
Cleared 510(K)
510(k) Number
K823256
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

ULTRA-ASEPT ANGIOGRAPHIC SYRINGE/SPARE

Page Type
Cleared 510(K)
510(k) Number
K823256
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