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FDA 510(k)

ALTERNATE SUPPLIERS FOR TENS ELECTRODE

K-Number: K872492 · 1987-07-22

ApplicantFranklin Sales & Mfg. Co.
Decision Date1987-07-22
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ALTERNATE SUPPLIERS FOR TENS ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Franklin Sales & Mfg. Co.. It received FDA 510(k) clearance on 1987-07-22 under 510(k) number K872492. 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 ALTERNATE SUPPLIERS FOR TENS ELECTRODE?

ALTERNATE SUPPLIERS FOR TENS ELECTRODE is a medical device that received FDA 510(k) clearance on 1987-07-22. The listed applicant is Franklin Sales & Mfg. Co.. The 510(k) number is K872492.

When did ALTERNATE SUPPLIERS FOR TENS ELECTRODE receive FDA 510(k) clearance?

ALTERNATE SUPPLIERS FOR TENS ELECTRODE received FDA 510(k) clearance on 1987-07-22, under 510(k) number K872492.

Who is the listed applicant for ALTERNATE SUPPLIERS FOR TENS ELECTRODE?

The FDA 510(k) record lists Franklin Sales & Mfg. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ALTERNATE SUPPLIERS FOR TENS ELECTRODE?

The FDA product code for ALTERNATE SUPPLIERS FOR TENS ELECTRODE 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 Franklin Sales & Mfg. Co. 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.

K822378TENS ELECTRODE

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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