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FDA 510(k)

AUTOMATIC ELECTRODE PLACEMENT BELT

K-Number: K810262 · 1981-03-11

ApplicantWallant Intl. Trade, Inc.
Decision Date1981-03-11
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

AUTOMATIC ELECTRODE PLACEMENT BELT is the device name listed in this FDA 510(k) record. The listed applicant is Wallant Intl. Trade, Inc.. It received FDA 510(k) clearance on 1981-03-11 under 510(k) number K810262. The device is classified under product code GXY. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTOMATIC ELECTRODE PLACEMENT BELT?

AUTOMATIC ELECTRODE PLACEMENT BELT is a medical device that received FDA 510(k) clearance on 1981-03-11. The listed applicant is Wallant Intl. Trade, Inc.. The 510(k) number is K810262.

When did AUTOMATIC ELECTRODE PLACEMENT BELT receive FDA 510(k) clearance?

AUTOMATIC ELECTRODE PLACEMENT BELT received FDA 510(k) clearance on 1981-03-11, under 510(k) number K810262.

Who is the listed applicant for AUTOMATIC ELECTRODE PLACEMENT BELT?

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

What is the FDA product code for AUTOMATIC ELECTRODE PLACEMENT BELT?

The FDA product code for AUTOMATIC ELECTRODE PLACEMENT BELT is GXY.

Related Clinical Trials

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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Other records listing Wallant Intl. Trade, 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.

K861119WALLANT NEUROLOGIX DUAL PUR NERVE/NEUROMUSCU STIMUK860847WALLANT NEUROLOGIX GENERAL PURPOSE TENS

Related Devices (Code: GXY)

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.

K262654Dexus Prosthetic System (MSL2, MSR2)Zhejiang Qiangnao Technology Co.,LtdK260578Ambu® NeurolineTM Cup MRI/CT (Models 72704/21US, 72704/23US, 72704/25US, 72704/27US) Ambu® NeurolineTM Cup MRI/CT-set (Models 72704/21-1010US, 72704/21-1010US, 72704/23-1010US, 72704/25-1010US, 72704/27-1010US) Ambu® NeurolineTM Cup MRI/CT-mini set (Models 72704/21-0301US, 72704/23-0301US, 72704/25-0301US, 72704/27-0301US)Ambu A/SK261442Charlotte ACC25 Surface Electrode Array; Charlotte ACC25 Reusable Surface Electrode ArrayCadwell Industries, Inc.K261522BioWave BioWrapsBiowave CorporationK253237Elde Medical Electrodes (T5/ 5 cm x 5cm electrode T10/ 5 cm x 10cm electrode)Elde Medikal Sanayi ve Ticaret Anonim SirketiK254183MR Conditional Cup ElectrodesTechnomed Europe

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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