MODIFICATION TO BD ULTRA-FINE III PEN NEEDLE
K-Number: K031200 · 2003-06-24
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Device Summary
Frequently Asked Questions
What is the MODIFICATION TO BD ULTRA-FINE III PEN NEEDLE?
MODIFICATION TO BD ULTRA-FINE III PEN NEEDLE is a medical device that received FDA 510(k) clearance on 2003-06-24. The listed applicant is Becton, Dickinson & CO. The 510(k) number is K031200.
When did MODIFICATION TO BD ULTRA-FINE III PEN NEEDLE receive FDA 510(k) clearance?
MODIFICATION TO BD ULTRA-FINE III PEN NEEDLE received FDA 510(k) clearance on 2003-06-24, under 510(k) number K031200.
Who is the listed applicant for MODIFICATION TO BD ULTRA-FINE III PEN NEEDLE?
The FDA 510(k) record lists Becton, Dickinson & CO as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODIFICATION TO BD ULTRA-FINE III PEN NEEDLE?
The FDA product code for MODIFICATION TO BD ULTRA-FINE III PEN NEEDLE is FMI.
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 & CO 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: FMI)
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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