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UTERINE TENTACULUM

Page Type
Cleared 510(K)
510(k) Number
K890379
510(k) Type
Traditional
Applicant
KINETIC MEDICAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/1989
Days to Decision
21 days

UTERINE TENTACULUM

Page Type
Cleared 510(K)
510(k) Number
K890379
510(k) Type
Traditional
Applicant
KINETIC MEDICAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/1989
Days to Decision
21 days