BD Epilor Syringe
K-Number: K210983 · 2022-05-19
ApplicantBecton, Dickinson and Company
Decision Date2022-05-19
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent
Device Summary
BD Epilor Syringe is a medical device manufactured by Becton, Dickinson and Company. It received FDA 510(k) clearance on 2022-05-19 under approval number K210983. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the BD Epilor Syringe?
BD Epilor Syringe is a medical device that received FDA 510(k) clearance on 2022-05-19. It is manufactured by Becton, Dickinson and Company. The 510(k) number is K210983.
When was BD Epilor Syringe approved by the FDA?
BD Epilor Syringe received FDA 510(k) clearance on 2022-05-19, under approval number K210983.
What company makes BD Epilor Syringe?
BD Epilor Syringe is manufactured by Becton, Dickinson and Company.
What is the FDA product code for BD Epilor Syringe?
The FDA product code for BD Epilor Syringe is CAZ.
Other Devices by Becton, Dickinson and Company
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K151589BD MAX CT/GC/TV, BD MAX INSTRUMENT
K151870BD U-500 INSULIN SYRINGE
K161553BD SafeAssist
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.