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FDA 510(k)

REPROCESSED ENDOSCOPIC ELECTRODES

K-Number: K012685 · 2002-02-14

ApplicantSterilmed, Inc.
Decision Date2002-02-14
Product CodeNLW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

REPROCESSED ENDOSCOPIC ELECTRODES is the device name listed in this FDA 510(k) record. The listed applicant is Sterilmed, Inc.. It received FDA 510(k) clearance on 2002-02-14 under 510(k) number K012685. The device is classified under product code NLW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REPROCESSED ENDOSCOPIC ELECTRODES?

REPROCESSED ENDOSCOPIC ELECTRODES is a medical device that received FDA 510(k) clearance on 2002-02-14. The listed applicant is Sterilmed, Inc.. The 510(k) number is K012685.

When did REPROCESSED ENDOSCOPIC ELECTRODES receive FDA 510(k) clearance?

REPROCESSED ENDOSCOPIC ELECTRODES received FDA 510(k) clearance on 2002-02-14, under 510(k) number K012685.

Who is the listed applicant for REPROCESSED ENDOSCOPIC ELECTRODES?

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 ENDOSCOPIC ELECTRODES?

The FDA product code for REPROCESSED ENDOSCOPIC ELECTRODES is NLW.

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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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