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Perineologic Access Needle

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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