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FDA 510(k)

ROTH NET RETRIEVER

K-Number: K122462 · 2012-09-11

ApplicantUnited States Endoscopy Group, Inc.
Decision Date2012-09-11
Product CodeFDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ROTH NET RETRIEVER 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 2012-09-11 under 510(k) number K122462. 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 ROTH NET RETRIEVER?

ROTH NET RETRIEVER is a medical device that received FDA 510(k) clearance on 2012-09-11. The listed applicant is United States Endoscopy Group, Inc.. The 510(k) number is K122462.

When did ROTH NET RETRIEVER receive FDA 510(k) clearance?

ROTH NET RETRIEVER received FDA 510(k) clearance on 2012-09-11, under 510(k) number K122462.

Who is the listed applicant for ROTH NET RETRIEVER?

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 ROTH NET RETRIEVER?

The FDA product code for ROTH NET RETRIEVER is FDI.

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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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