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FDA 510(k)

INJECTOR NEEDLE/SNARE

K-Number: K040961 · 2004-07-08

ApplicantUnited States Endoscopy Group, Inc.
Decision Date2004-07-08
Product CodeFDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

INJECTOR NEEDLE/SNARE is the device name listed in this FDA 510(k) record. The listed applicant is United States Endoscopy Group, Inc.. It received FDA 510(k) clearance on 2004-07-08 under 510(k) number K040961. The device is classified under product code FDI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INJECTOR NEEDLE/SNARE?

INJECTOR NEEDLE/SNARE is a medical device that received FDA 510(k) clearance on 2004-07-08. The listed applicant is United States Endoscopy Group, Inc.. The 510(k) number is K040961.

When did INJECTOR NEEDLE/SNARE receive FDA 510(k) clearance?

INJECTOR NEEDLE/SNARE received FDA 510(k) clearance on 2004-07-08, under 510(k) number K040961.

Who is the listed applicant for INJECTOR NEEDLE/SNARE?

The FDA 510(k) record lists United States Endoscopy Group, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INJECTOR NEEDLE/SNARE?

The FDA product code for INJECTOR NEEDLE/SNARE is FDI.

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Related Devices (Code: FDI)

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.

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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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