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BD SoloShot Mini Syringe/ BD Auto Disable Syringe

Page Type
Cleared 510(K)
510(k) Number
K201234
510(k) Type
Traditional
Applicant
Becton, Dickinson, and Company
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/15/2020
Days to Decision
69 days
Submission Type
Summary

BD SoloShot Mini Syringe/ BD Auto Disable Syringe

Page Type
Cleared 510(K)
510(k) Number
K201234
510(k) Type
Traditional
Applicant
Becton, Dickinson, and Company
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/15/2020
Days to Decision
69 days
Submission Type
Summary