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CATHETER/HEMOSTATIC/GERIATRIC

Page Type
Cleared 510(K)
510(k) Number
K780062
510(k) Type
Traditional
Applicant
KENDALL RESEARCH CENTER
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/14/1978
Days to Decision
33 days

CATHETER/HEMOSTATIC/GERIATRIC

Page Type
Cleared 510(K)
510(k) Number
K780062
510(k) Type
Traditional
Applicant
KENDALL RESEARCH CENTER
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/14/1978
Days to Decision
33 days