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AMNISURE FETAL MEMBRANES RUPTURE TEST, MODEL FMRT-1

Page Type
Cleared 510(K)
510(k) Number
K081767
510(k) Type
Traditional
Applicant
Amnisure International, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/2009
Days to Decision
203 days
Submission Type
Statement

AMNISURE FETAL MEMBRANES RUPTURE TEST, MODEL FMRT-1

Page Type
Cleared 510(K)
510(k) Number
K081767
510(k) Type
Traditional
Applicant
Amnisure International, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/2009
Days to Decision
203 days
Submission Type
Statement