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FDA 510(k)

EC SINGLE USE, POLYPECTOMY SNARE

K-Number: K123223 · 2013-01-10

ApplicantEndochoice, Inc.
Decision Date2013-01-10
Product CodeFDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

EC SINGLE USE, POLYPECTOMY SNARE is the device name listed in this FDA 510(k) record. The listed applicant is Endochoice, Inc.. It received FDA 510(k) clearance on 2013-01-10 under 510(k) number K123223. 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 EC SINGLE USE, POLYPECTOMY SNARE?

EC SINGLE USE, POLYPECTOMY SNARE is a medical device that received FDA 510(k) clearance on 2013-01-10. The listed applicant is Endochoice, Inc.. The 510(k) number is K123223.

When did EC SINGLE USE, POLYPECTOMY SNARE receive FDA 510(k) clearance?

EC SINGLE USE, POLYPECTOMY SNARE received FDA 510(k) clearance on 2013-01-10, under 510(k) number K123223.

Who is the listed applicant for EC SINGLE USE, POLYPECTOMY SNARE?

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

What is the FDA product code for EC SINGLE USE, POLYPECTOMY SNARE?

The FDA product code for EC SINGLE USE, POLYPECTOMY 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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