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FDA 510(k)

WALLACH LOOP ELECTRODE

K-Number: K020711 · 2002-06-03

ApplicantWallach Surgical Devices, Inc.
Decision Date2002-06-03
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

WALLACH LOOP ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Wallach Surgical Devices, Inc.. It received FDA 510(k) clearance on 2002-06-03 under 510(k) number K020711. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WALLACH LOOP ELECTRODE?

WALLACH LOOP ELECTRODE is a medical device that received FDA 510(k) clearance on 2002-06-03. The listed applicant is Wallach Surgical Devices, Inc.. The 510(k) number is K020711.

When did WALLACH LOOP ELECTRODE receive FDA 510(k) clearance?

WALLACH LOOP ELECTRODE received FDA 510(k) clearance on 2002-06-03, under 510(k) number K020711.

Who is the listed applicant for WALLACH LOOP ELECTRODE?

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

What is the FDA product code for WALLACH LOOP ELECTRODE?

The FDA product code for WALLACH LOOP ELECTRODE is GEI.

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Other records listing Wallach Surgical Devices, 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.

K021224ENDOCERVICAL BLOCK NEEDLEK000768WALLACH QUANTUM 500 ELECTROSURGICAL GENERATORK992736WALLACH'S ULTIMATE REUSABLE, PLASTIC VAGINAL SPECULUMK991669PMS 750 FINGERSWITCHK983840WALLACH QUANTUM 500 ELECTROSURGICAL GENERATOR (PROPOSED)K984306`THE INSEMINATOR' (PROPOSED)

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Related Devices (Code: GEI)

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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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