FDA 510(k)

REPROCESSED ELECTROSURGICAL ELECTRODE

K-Number: K012684 · 2002-01-18

Decision Date2002-01-18

Product CodeJOS

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

REPROCESSED ELECTROSURGICAL ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Sterilmed, Inc.. It received FDA 510(k) clearance on 2002-01-18 under 510(k) number K012684. The device is classified under product code JOS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REPROCESSED ELECTROSURGICAL ELECTRODE?

REPROCESSED ELECTROSURGICAL ELECTRODE is a medical device that received FDA 510(k) clearance on 2002-01-18. The listed applicant is Sterilmed, Inc.. The 510(k) number is K012684.

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

REPROCESSED ELECTROSURGICAL ELECTRODE received FDA 510(k) clearance on 2002-01-18, under 510(k) number K012684.

Who is the listed applicant for REPROCESSED ELECTROSURGICAL ELECTRODE?

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

What is the FDA product code for REPROCESSED ELECTROSURGICAL ELECTRODE?

The FDA product code for REPROCESSED ELECTROSURGICAL ELECTRODE is JOS.

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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.