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INTRAUTERINE HEMOSTASIS BALLOON STENT

Page Type
Cleared 510(K)
510(k) Number
K863439
510(k) Type
Traditional
Applicant
MENTOR CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/2/1987
Days to Decision
270 days

INTRAUTERINE HEMOSTASIS BALLOON STENT

Page Type
Cleared 510(K)
510(k) Number
K863439
510(k) Type
Traditional
Applicant
MENTOR CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/2/1987
Days to Decision
270 days