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CERVICAL DILATOR

Page Type
Cleared 510(K)
510(k) Number
K811568
510(k) Type
Traditional
Applicant
GYNEMETRICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/16/1981
Days to Decision
42 days

CERVICAL DILATOR

Page Type
Cleared 510(K)
510(k) Number
K811568
510(k) Type
Traditional
Applicant
GYNEMETRICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/16/1981
Days to Decision
42 days