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FDA 510(k)

SINGLE USE GROUNDING PAD

K-Number: K132136 · 2013-09-06

ApplicantLccs Products Limited
Decision Date2013-09-06
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SINGLE USE GROUNDING PAD is the device name listed in this FDA 510(k) record. The listed applicant is Lccs Products Limited. It received FDA 510(k) clearance on 2013-09-06 under 510(k) number K132136. 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 SINGLE USE GROUNDING PAD?

SINGLE USE GROUNDING PAD is a medical device that received FDA 510(k) clearance on 2013-09-06. The listed applicant is Lccs Products Limited. The 510(k) number is K132136.

When did SINGLE USE GROUNDING PAD receive FDA 510(k) clearance?

SINGLE USE GROUNDING PAD received FDA 510(k) clearance on 2013-09-06, under 510(k) number K132136.

Who is the listed applicant for SINGLE USE GROUNDING PAD?

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

What is the FDA product code for SINGLE USE GROUNDING PAD?

The FDA product code for SINGLE USE GROUNDING PAD is GEI.

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Other records listing Lccs Products Limited as applicant

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K191293LCCS VC-S RF CannulaK152642LCCS Disposable RF Electrode, LCCS Reusable RF ElectrodeK131006ANESTHESIA CONDUCTION NEEDLESK112231LCCS INSULATED SPINAL NEEDLE (RF CANNULA)

Related Devices (Code: GEI)

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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