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FDA 510(k)

ULTRABLATOR ELECTRODE

K-Number: K993885 · 2000-02-10

ApplicantLinvatec Corp.
Decision Date2000-02-10
Product CodeJOS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ULTRABLATOR ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Linvatec Corp.. It received FDA 510(k) clearance on 2000-02-10 under 510(k) number K993885. 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 ULTRABLATOR ELECTRODE?

ULTRABLATOR ELECTRODE is a medical device that received FDA 510(k) clearance on 2000-02-10. The listed applicant is Linvatec Corp.. The 510(k) number is K993885.

When did ULTRABLATOR ELECTRODE receive FDA 510(k) clearance?

ULTRABLATOR ELECTRODE received FDA 510(k) clearance on 2000-02-10, under 510(k) number K993885.

Who is the listed applicant for ULTRABLATOR ELECTRODE?

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

What is the FDA product code for ULTRABLATOR ELECTRODE?

The FDA product code for ULTRABLATOR ELECTRODE is JOS.

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Other records listing Linvatec Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: JOS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K161600Resection ElectrodesOlympus Winter & Ibe GmbHK050923LIGHTWAVE INTEGRATED ELECTRODE ABLATOR AND LIGHT WAVE INTEGRATED ELECTRODE SUCTION ABLATORConmed LinvatecK012684REPROCESSED ELECTROSURGICAL ELECTRODESterilmed, Inc.K011515MEDLINE GROUNDING PADMedline Industries, Inc.K003403ENDOSCOPIC MONOPOLAREECTRODE, MODEL EME- 1000 TO 1999Highland / Marietta, Inc.K000333STANDARD & EXTENDED BLADE, STANDARD & EXTENDED NEEDLE, STANDARD & EXTENDED BALL, MODIFIED STANDARD & EXTENDED BLADE, MODTriad Surgical Technologies, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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