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FDA 510(k)

CERVICAL LOOP ELECTRODE & ROLLERBALL ELECTRODE

K-Number: K923628 · 1994-02-22

ApplicantBruce Mclucas
Decision Date1994-02-22
Product CodeHGI
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CERVICAL LOOP ELECTRODE & ROLLERBALL ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Bruce Mclucas. It received FDA 510(k) clearance on 1994-02-22 under 510(k) number K923628. The device is classified under product code HGI. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CERVICAL LOOP ELECTRODE & ROLLERBALL ELECTRODE?

CERVICAL LOOP ELECTRODE & ROLLERBALL ELECTRODE is a medical device that received FDA 510(k) clearance on 1994-02-22. The listed applicant is Bruce Mclucas. The 510(k) number is K923628.

When did CERVICAL LOOP ELECTRODE & ROLLERBALL ELECTRODE receive FDA 510(k) clearance?

CERVICAL LOOP ELECTRODE & ROLLERBALL ELECTRODE received FDA 510(k) clearance on 1994-02-22, under 510(k) number K923628.

Who is the listed applicant for CERVICAL LOOP ELECTRODE & ROLLERBALL ELECTRODE?

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

What is the FDA product code for CERVICAL LOOP ELECTRODE & ROLLERBALL ELECTRODE?

The FDA product code for CERVICAL LOOP ELECTRODE & ROLLERBALL ELECTRODE is HGI.

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Related Devices (Code: HGI)

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.

K202915IRIS Thermocoagulator and Digital ColposcopeLiger Medical, LLCK152843Liger Medical HTU-110Liger Medical, LLCK121881DOMAIN SURGICAL SYSTEMDomain Surgical, Inc.K070877ENDOCERVICAL ELECTRODE # 2Modern Medical Equipment Mfg., Ltd.K061651FISCHER CONE BIOPSY EXCISOR, MODELS 900-150, 151, 152, 154, 155, 157 AND 158Apple Medical Corp.K022593THOMAS MEDICAL ELECTRODESThomas Medical, 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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