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FDA 510(k)

DIGITAL RING ELECTRDE

K-Number: K991771 · 1999-08-18

ApplicantNeuro Supplies, Inc.
Decision Date1999-08-18
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

DIGITAL RING ELECTRDE is the device name listed in this FDA 510(k) record. The listed applicant is Neuro Supplies, Inc.. It received FDA 510(k) clearance on 1999-08-18 under 510(k) number K991771. 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 DIGITAL RING ELECTRDE?

DIGITAL RING ELECTRDE is a medical device that received FDA 510(k) clearance on 1999-08-18. The listed applicant is Neuro Supplies, Inc.. The 510(k) number is K991771.

When did DIGITAL RING ELECTRDE receive FDA 510(k) clearance?

DIGITAL RING ELECTRDE received FDA 510(k) clearance on 1999-08-18, under 510(k) number K991771.

Who is the listed applicant for DIGITAL RING ELECTRDE?

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

What is the FDA product code for DIGITAL RING ELECTRDE?

The FDA product code for DIGITAL RING ELECTRDE 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 Neuro Supplies, 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.

K991772CUTANEOUS (DISC) ELECTRODEK991770CUTANEOUS (GROUND) ELECTRODEK991769CUTANEOUS (BAR) ELECTRODEK942921NEUROLINK EEG/EP/EMG SURFACE ELECTRODES

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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