FDA 510(k)

USA ELITE SYSTEM VAPORTRODE VAPORIZATION ELECTRODE AND VAPORTOME RESECTION ELECTRODE

K-Number: K973820 · 1998-05-12

Decision Date1998-05-12

Product CodeFAS

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

USA ELITE SYSTEM VAPORTRODE VAPORIZATION ELECTRODE AND VAPORTOME RESECTION ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Circon Corp.. It received FDA 510(k) clearance on 1998-05-12 under 510(k) number K973820. The device is classified under product code FAS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the USA ELITE SYSTEM VAPORTRODE VAPORIZATION ELECTRODE AND VAPORTOME RESECTION ELECTRODE?

USA ELITE SYSTEM VAPORTRODE VAPORIZATION ELECTRODE AND VAPORTOME RESECTION ELECTRODE is a medical device that received FDA 510(k) clearance on 1998-05-12. The listed applicant is Circon Corp.. The 510(k) number is K973820.

When did USA ELITE SYSTEM VAPORTRODE VAPORIZATION ELECTRODE AND VAPORTOME RESECTION ELECTRODE receive FDA 510(k) clearance?

USA ELITE SYSTEM VAPORTRODE VAPORIZATION ELECTRODE AND VAPORTOME RESECTION ELECTRODE received FDA 510(k) clearance on 1998-05-12, under 510(k) number K973820.

Who is the listed applicant for USA ELITE SYSTEM VAPORTRODE VAPORIZATION ELECTRODE AND VAPORTOME RESECTION ELECTRODE?

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

What is the FDA product code for USA ELITE SYSTEM VAPORTRODE VAPORIZATION ELECTRODE AND VAPORTOME RESECTION ELECTRODE?

The FDA product code for USA ELITE SYSTEM VAPORTRODE VAPORIZATION ELECTRODE AND VAPORTOME RESECTION ELECTRODE is FAS.

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Other records listing Circon Corp. as applicant

K992544TRANSVAGINAL HYDRO LAPAROSCOPY (THL) SYSTEM K992126CIRCON SURGIFLEX WAVE TSUNAMI SUCTION-IRRIGATION SYSTEM K981611SNAP-N-PEEL INTRODUCERS K980972RIGID CULDOSCOPE AND ACCESSORIES K964594VAPORTRODE VAPORIZATION ELECTRODE -GROOVED/FLUTED/SPIKED(GVE-B,GVE-F,GVE-S) & VAPORTOMME VAPORIZATION LOOP (GVE-LG)

Related Devices (Code: FAS)

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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.