BD Insulin Syringe (0.3mL)
K-Number: K212499 · 2022-03-09
Device Summary
Frequently Asked Questions
What is the BD Insulin Syringe (0.3mL)?
BD Insulin Syringe (0.3mL) is a medical device that received FDA 510(k) clearance on 2022-03-09. The listed applicant is Becton, Dickinson and Company. The 510(k) number is K212499.
When did BD Insulin Syringe (0.3mL) receive FDA 510(k) clearance?
BD Insulin Syringe (0.3mL) received FDA 510(k) clearance on 2022-03-09, under 510(k) number K212499.
Who is the listed applicant for BD Insulin Syringe (0.3mL)?
The FDA 510(k) record lists Becton, Dickinson and Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BD Insulin Syringe (0.3mL)?
The FDA product code for BD Insulin Syringe (0.3mL) is FMF.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Becton, Dickinson and Company as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: FMF)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.