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GYNESCOPE

Page Type
Cleared 510(K)
510(k) Number
K880195
510(k) Type
Traditional
Applicant
MEDGYN PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/14/1988
Days to Decision
48 days

GYNESCOPE

Page Type
Cleared 510(K)
510(k) Number
K880195
510(k) Type
Traditional
Applicant
MEDGYN PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/14/1988
Days to Decision
48 days