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MICROGYN PLUS STIMULATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K013141
510(k) Type
Traditional
Applicant
HOLLISTER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/19/2001
Days to Decision
90 days
Submission Type
Summary

MICROGYN PLUS STIMULATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K013141
510(k) Type
Traditional
Applicant
HOLLISTER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/19/2001
Days to Decision
90 days
Submission Type
Summary