Last synced on 14 November 2025 at 11:06 pm

VAGINAL 2 ELECTRODE STIMULATION/EMG PROBE-SMALL

Page Type
Cleared 510(K)
510(k) Number
K970602
510(k) Type
Traditional
Applicant
HOLLISTER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/15/1997
Days to Decision
56 days
Submission Type
Summary

VAGINAL 2 ELECTRODE STIMULATION/EMG PROBE-SMALL

Page Type
Cleared 510(K)
510(k) Number
K970602
510(k) Type
Traditional
Applicant
HOLLISTER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/15/1997
Days to Decision
56 days
Submission Type
Summary