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FDA 510(k)

DISPOSABLE ELECTROSURGERY BALL ELECTRODE

K-Number: K925708 · 1993-04-20

ApplicantBeacon Laboratories, Inc.
Decision Date1993-04-20
Product CodeDWG
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE ELECTROSURGERY BALL ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Beacon Laboratories, Inc.. It received FDA 510(k) clearance on 1993-04-20 under 510(k) number K925708. The device is classified under product code DWG. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE ELECTROSURGERY BALL ELECTRODE?

DISPOSABLE ELECTROSURGERY BALL ELECTRODE is a medical device that received FDA 510(k) clearance on 1993-04-20. The listed applicant is Beacon Laboratories, Inc.. The 510(k) number is K925708.

When did DISPOSABLE ELECTROSURGERY BALL ELECTRODE receive FDA 510(k) clearance?

DISPOSABLE ELECTROSURGERY BALL ELECTRODE received FDA 510(k) clearance on 1993-04-20, under 510(k) number K925708.

Who is the listed applicant for DISPOSABLE ELECTROSURGERY BALL ELECTRODE?

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

What is the FDA product code for DISPOSABLE ELECTROSURGERY BALL ELECTRODE?

The FDA product code for DISPOSABLE ELECTROSURGERY BALL ELECTRODE is DWG.

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Other records listing Beacon Laboratories, 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.

K930243FLEXIBLE EXTENDERK930497ARGON HANDPIECESK922289SESQUIPOLAR(TM) MIS ELECTRODEK925619DISPOSABLE HAND-SWITCHING ESU PENCILK915788MIS ELECTROSURGICAL ELECTRODESK920100GSU HANDPIECE ADAPTER

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Related Devices (Code: DWG)

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.

K942823MAHE INSTRUMENTSMahe Intl., Inc.K932345TECH-SWITCH ELECTROSURGICAL PENCIL, SINGLE USEConmedcorpK931215HAND-TROL SAspen Labs

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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