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FDA 510(k)

THE DOCTOR'S CHOICE ELECTRODE

K-Number: K895737 · 1989-11-08

ApplicantThe Skin Care Centre
Decision Date1989-11-08
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

THE DOCTOR'S CHOICE ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is The Skin Care Centre. It received FDA 510(k) clearance on 1989-11-08 under 510(k) number K895737. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE DOCTOR'S CHOICE ELECTRODE?

THE DOCTOR'S CHOICE ELECTRODE is a medical device that received FDA 510(k) clearance on 1989-11-08. The listed applicant is The Skin Care Centre. The 510(k) number is K895737.

When did THE DOCTOR'S CHOICE ELECTRODE receive FDA 510(k) clearance?

THE DOCTOR'S CHOICE ELECTRODE received FDA 510(k) clearance on 1989-11-08, under 510(k) number K895737.

Who is the listed applicant for THE DOCTOR'S CHOICE ELECTRODE?

The FDA 510(k) record lists The Skin Care Centre as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE DOCTOR'S CHOICE ELECTRODE?

The FDA product code for THE DOCTOR'S CHOICE ELECTRODE is GEI.

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Official Source

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