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MONITORING KIT, CENTRAL VENOUS PRESSURE

Page Type
Cleared 510(K)
510(k) Number
K770290
510(k) Type
Traditional
Applicant
ARGON MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/1977
Days to Decision
29 days

MONITORING KIT, CENTRAL VENOUS PRESSURE

Page Type
Cleared 510(K)
510(k) Number
K770290
510(k) Type
Traditional
Applicant
ARGON MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/1977
Days to Decision
29 days