Last synced on 14 November 2025 at 11:06 pm

Perineologic Access Needle

Page Type
Cleared 510(K)
510(k) Number
K160423
510(k) Type
Traditional
Applicant
Corbin Clinical Resources, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/2016
Days to Decision
199 days
Submission Type
Summary

Perineologic Access Needle

Page Type
Cleared 510(K)
510(k) Number
K160423
510(k) Type
Traditional
Applicant
Corbin Clinical Resources, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/2016
Days to Decision
199 days
Submission Type
Summary