Last synced on 4 February 2023 at 10:33 pm

IUI, MODEL 4220; SMOOZE, MODEL 4225, L; SEMINOR, MODEL 4502 A, B

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013501
510(k) Type
Traditional
Applicant
GYNETICS MEDICAL PRODUCTS NV
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/30/2001
Days to Decision
39 days
Submission Type
Statement

IUI, MODEL 4220; SMOOZE, MODEL 4225, L; SEMINOR, MODEL 4502 A, B

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013501
510(k) Type
Traditional
Applicant
GYNETICS MEDICAL PRODUCTS NV
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/30/2001
Days to Decision
39 days
Submission Type
Statement