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FDA 510(k)

WUZHOU SYRINGE, WITH/WITHOUT NEEDLE

K-Number: K060211 · 2006-02-10

Decision Date2006-02-10
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

WUZHOU SYRINGE, WITH/WITHOUT NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Wenzhou Wuzhou Group Co. , Ltd.. It received FDA 510(k) clearance on 2006-02-10 under 510(k) number K060211. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WUZHOU SYRINGE, WITH/WITHOUT NEEDLE?

WUZHOU SYRINGE, WITH/WITHOUT NEEDLE is a medical device that received FDA 510(k) clearance on 2006-02-10. The listed applicant is Wenzhou Wuzhou Group Co. , Ltd.. The 510(k) number is K060211.

When did WUZHOU SYRINGE, WITH/WITHOUT NEEDLE receive FDA 510(k) clearance?

WUZHOU SYRINGE, WITH/WITHOUT NEEDLE received FDA 510(k) clearance on 2006-02-10, under 510(k) number K060211.

Who is the listed applicant for WUZHOU SYRINGE, WITH/WITHOUT NEEDLE?

The FDA 510(k) record lists Wenzhou Wuzhou Group Co. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WUZHOU SYRINGE, WITH/WITHOUT NEEDLE?

The FDA product code for WUZHOU SYRINGE, WITH/WITHOUT NEEDLE 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.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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