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FDA 510(k)

HIGH SPEED MAGNETIC STIMULATOR

K-Number: K905059 · 1991-09-18

ApplicantCadwell Laboratories, Inc.
Decision Date1991-09-18
Product CodeGWF
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

HIGH SPEED MAGNETIC 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 1991-09-18 under 510(k) number K905059. 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 HIGH SPEED MAGNETIC STIMULATOR?

HIGH SPEED MAGNETIC STIMULATOR is a medical device that received FDA 510(k) clearance on 1991-09-18. The listed applicant is Cadwell Laboratories, Inc.. The 510(k) number is K905059.

When did HIGH SPEED MAGNETIC STIMULATOR receive FDA 510(k) clearance?

HIGH SPEED MAGNETIC STIMULATOR received FDA 510(k) clearance on 1991-09-18, under 510(k) number K905059.

Who is the listed applicant for HIGH SPEED MAGNETIC 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 HIGH SPEED MAGNETIC STIMULATOR?

The FDA product code for HIGH SPEED MAGNETIC STIMULATOR is GWF.

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Other records listing Cadwell Laboratories, 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.

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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