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CENTRAL CATHETER KIT

Page Type
Cleared 510(K)
510(k) Number
K780673
510(k) Type
Traditional
Applicant
ARGON MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/16/1978
Days to Decision
22 days

CENTRAL CATHETER KIT

Page Type
Cleared 510(K)
510(k) Number
K780673
510(k) Type
Traditional
Applicant
ARGON MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/16/1978
Days to Decision
22 days