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FDA 510(k)

Rotatable Snares

K-Number: K160637 · 2016-03-30

ApplicantBoston Scientific Corporation
Decision Date2016-03-30
Product CodeFDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Rotatable Snares is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Corporation. It received FDA 510(k) clearance on 2016-03-30 under 510(k) number K160637. 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 Rotatable Snares?

Rotatable Snares is a medical device that received FDA 510(k) clearance on 2016-03-30. The listed applicant is Boston Scientific Corporation. The 510(k) number is K160637.

When did Rotatable Snares receive FDA 510(k) clearance?

Rotatable Snares received FDA 510(k) clearance on 2016-03-30, under 510(k) number K160637.

Who is the listed applicant for Rotatable Snares?

The FDA 510(k) record lists Boston Scientific Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Rotatable Snares?

The FDA product code for Rotatable Snares is FDI.

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Related Devices (Code: 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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