BECTON DICKINSON SYRINGSE
K-Number: K954064 · 1995-11-21
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Device Summary
Frequently Asked Questions
What is the BECTON DICKINSON SYRINGSE?
BECTON DICKINSON SYRINGSE is a medical device that received FDA 510(k) clearance on 1995-11-21. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K954064.
When did BECTON DICKINSON SYRINGSE receive FDA 510(k) clearance?
BECTON DICKINSON SYRINGSE received FDA 510(k) clearance on 1995-11-21, under 510(k) number K954064.
Who is the listed applicant for BECTON DICKINSON SYRINGSE?
The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BECTON DICKINSON SYRINGSE?
The FDA product code for BECTON DICKINSON SYRINGSE 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 Bd Becton Dickinson Vacutainer Systems Preanalytic 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.
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