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FDA 510(k)

EES 10 ELECTRODELESS ELECTRICAL STIMULATOR

K-Number: K863175 · 1987-01-13

ApplicantCadwell Laboratories, Inc.
Decision Date1987-01-13
Product CodeGWF
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

EES 10 ELECTRODELESS ELECTRICAL STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Cadwell Laboratories, Inc.. It received FDA 510(k) clearance on 1987-01-13 under 510(k) number K863175. The device is classified under product code GWF. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EES 10 ELECTRODELESS ELECTRICAL STIMULATOR?

EES 10 ELECTRODELESS ELECTRICAL STIMULATOR is a medical device that received FDA 510(k) clearance on 1987-01-13. The listed applicant is Cadwell Laboratories, Inc.. The 510(k) number is K863175.

When did EES 10 ELECTRODELESS ELECTRICAL STIMULATOR receive FDA 510(k) clearance?

EES 10 ELECTRODELESS ELECTRICAL STIMULATOR received FDA 510(k) clearance on 1987-01-13, under 510(k) number K863175.

Who is the listed applicant for EES 10 ELECTRODELESS ELECTRICAL STIMULATOR?

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

What is the FDA product code for EES 10 ELECTRODELESS ELECTRICAL STIMULATOR?

The FDA product code for EES 10 ELECTRODELESS ELECTRICAL STIMULATOR is GWF.

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Other records listing Cadwell Laboratories, Inc. as applicant

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K061706CADWELL EASYNET OXIMETER MODULEK061705CADWELL EASYNET NASAL PRESSURE MODULEK042350TES-1 CONSTANT VOLTAGE ELECTRICAL STIMULATORK040986CADWELL LIMB MOVEMENT MODULEK040932EASYNET BODY POSITION MODULEK971214KILOWIN

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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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