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FDA 510(k)

CANADY VIEIRA HYBRID PLASMA SCALPEL

K-Number: K113500 · 2011-12-09

ApplicantUs Medical Innovations, LLC
Decision Date2011-12-09
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CANADY VIEIRA HYBRID PLASMA SCALPEL is the device name listed in this FDA 510(k) record. The listed applicant is Us Medical Innovations, LLC. It received FDA 510(k) clearance on 2011-12-09 under 510(k) number K113500. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CANADY VIEIRA HYBRID PLASMA SCALPEL?

CANADY VIEIRA HYBRID PLASMA SCALPEL is a medical device that received FDA 510(k) clearance on 2011-12-09. The listed applicant is Us Medical Innovations, LLC. The 510(k) number is K113500.

When did CANADY VIEIRA HYBRID PLASMA SCALPEL receive FDA 510(k) clearance?

CANADY VIEIRA HYBRID PLASMA SCALPEL received FDA 510(k) clearance on 2011-12-09, under 510(k) number K113500.

Who is the listed applicant for CANADY VIEIRA HYBRID PLASMA SCALPEL?

The FDA 510(k) record lists Us Medical Innovations, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CANADY VIEIRA HYBRID PLASMA SCALPEL?

The FDA product code for CANADY VIEIRA HYBRID PLASMA SCALPEL is GEI.

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Other records listing Us Medical Innovations, LLC as applicant

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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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