FDA 510(k)

FLEXIBLE LOOP ELECTROSURGICAL ELECTRODE

K-Number: K070275 · 2007-03-09

Decision Date2007-03-09

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

FLEXIBLE LOOP ELECTROSURGICAL ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Rubicor Medical, Inc.. It received FDA 510(k) clearance on 2007-03-09 under 510(k) number K070275. 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 FLEXIBLE LOOP ELECTROSURGICAL ELECTRODE?

FLEXIBLE LOOP ELECTROSURGICAL ELECTRODE is a medical device that received FDA 510(k) clearance on 2007-03-09. The listed applicant is Rubicor Medical, Inc.. The 510(k) number is K070275.

When did FLEXIBLE LOOP ELECTROSURGICAL ELECTRODE receive FDA 510(k) clearance?

FLEXIBLE LOOP ELECTROSURGICAL ELECTRODE received FDA 510(k) clearance on 2007-03-09, under 510(k) number K070275.

Who is the listed applicant for FLEXIBLE LOOP ELECTROSURGICAL ELECTRODE?

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

What is the FDA product code for FLEXIBLE LOOP ELECTROSURGICAL ELECTRODE?

The FDA product code for FLEXIBLE LOOP ELECTROSURGICAL ELECTRODE is GEI.

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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.