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TRANSLUMBAR AORTOGRAPHY NEEDLE CATHETER

Page Type
Cleared 510(K)
510(k) Number
K884375
510(k) Type
Traditional
Applicant
ARGON MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/11/1989
Days to Decision
85 days

TRANSLUMBAR AORTOGRAPHY NEEDLE CATHETER

Page Type
Cleared 510(K)
510(k) Number
K884375
510(k) Type
Traditional
Applicant
ARGON MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/11/1989
Days to Decision
85 days