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FDA 510(k)

SENTRY DISPOSABLE DISPERSIVE ELECTRODE

K-Number: K955636 · 1996-03-27

ApplicantSentry Medical Products, Inc.
Decision Date1996-03-27
Product CodeJOS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SENTRY DISPOSABLE DISPERSIVE ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Sentry Medical Products, Inc.. It received FDA 510(k) clearance on 1996-03-27 under 510(k) number K955636. 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 SENTRY DISPOSABLE DISPERSIVE ELECTRODE?

SENTRY DISPOSABLE DISPERSIVE ELECTRODE is a medical device that received FDA 510(k) clearance on 1996-03-27. The listed applicant is Sentry Medical Products, Inc.. The 510(k) number is K955636.

When did SENTRY DISPOSABLE DISPERSIVE ELECTRODE receive FDA 510(k) clearance?

SENTRY DISPOSABLE DISPERSIVE ELECTRODE received FDA 510(k) clearance on 1996-03-27, under 510(k) number K955636.

Who is the listed applicant for SENTRY DISPOSABLE DISPERSIVE ELECTRODE?

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

What is the FDA product code for SENTRY DISPOSABLE DISPERSIVE ELECTRODE?

The FDA product code for SENTRY DISPOSABLE DISPERSIVE ELECTRODE is JOS.

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Other records listing Sentry Medical Products, Inc. as applicant

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Related Devices (Code: JOS)

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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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