MAEDA NEW NEEDLE DISPOSABLE
K-Number: K000581 · 2001-02-23
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Device Summary
Frequently Asked Questions
What is the MAEDA NEW NEEDLE DISPOSABLE?
MAEDA NEW NEEDLE DISPOSABLE is a medical device that received FDA 510(k) clearance on 2001-02-23. The listed applicant is Maeda Toyokichi Shoten. The 510(k) number is K000581.
When did MAEDA NEW NEEDLE DISPOSABLE receive FDA 510(k) clearance?
MAEDA NEW NEEDLE DISPOSABLE received FDA 510(k) clearance on 2001-02-23, under 510(k) number K000581.
Who is the listed applicant for MAEDA NEW NEEDLE DISPOSABLE?
The FDA 510(k) record lists Maeda Toyokichi Shoten as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MAEDA NEW NEEDLE DISPOSABLE?
The FDA product code for MAEDA NEW NEEDLE DISPOSABLE is MQX.
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 Maeda Toyokichi Shoten 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: MQX)
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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