Last synced on 14 November 2025 at 11:06 pm

FENESTRATED NERVE BLOCK NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K113662
510(k) Type
Traditional
Applicant
IMD INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/20/2012
Days to Decision
135 days
Submission Type
Summary

FENESTRATED NERVE BLOCK NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K113662
510(k) Type
Traditional
Applicant
IMD INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/20/2012
Days to Decision
135 days
Submission Type
Summary