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Ranfac Cartilage Biopsy Needle

Page Type
Cleared 510(K)
510(k) Number
K183146
510(k) Type
Traditional
Applicant
Ranfac Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/25/2019
Days to Decision
163 days
Submission Type
Summary

Ranfac Cartilage Biopsy Needle

Page Type
Cleared 510(K)
510(k) Number
K183146
510(k) Type
Traditional
Applicant
Ranfac Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/25/2019
Days to Decision
163 days
Submission Type
Summary