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FDA 510(k)

INFANT ELECTROSURGICAL DISPERSIVE ELECTRODE

K-Number: K882421 · 1988-06-30

ApplicantDermacare Products, Inc.
Decision Date1988-06-30
Product CodeJOS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

INFANT ELECTROSURGICAL DISPERSIVE ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Dermacare Products, Inc.. It received FDA 510(k) clearance on 1988-06-30 under 510(k) number K882421. 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 INFANT ELECTROSURGICAL DISPERSIVE ELECTRODE?

INFANT ELECTROSURGICAL DISPERSIVE ELECTRODE is a medical device that received FDA 510(k) clearance on 1988-06-30. The listed applicant is Dermacare Products, Inc.. The 510(k) number is K882421.

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

INFANT ELECTROSURGICAL DISPERSIVE ELECTRODE received FDA 510(k) clearance on 1988-06-30, under 510(k) number K882421.

Who is the listed applicant for INFANT ELECTROSURGICAL DISPERSIVE ELECTRODE?

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

What is the FDA product code for INFANT ELECTROSURGICAL DISPERSIVE ELECTRODE?

The FDA product code for INFANT ELECTROSURGICAL DISPERSIVE ELECTRODE is JOS.

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Other records listing Dermacare Products, Inc. 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.

K882494ELAN-E DISPOSALBE DRAPEK871910SURGITEK DISPOSABLE BIPOLAR CORDK863279SURGI-TEK TUBE POSITIONERK863280DERMAMARKERK863278SURGI-WIPESK862367PRO-CLEAN

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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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