FDA 510(k)

NEOMED NON GEL-R TOTAL ADHESIVE CONDUCT. ELECTRODE

K-Number: K863360 · 1986-09-12

Decision Date1986-09-12

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

NEOMED NON GEL-R TOTAL ADHESIVE CONDUCT. ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Richards Medical Co., Inc.. It received FDA 510(k) clearance on 1986-09-12 under 510(k) number K863360. 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 NEOMED NON GEL-R TOTAL ADHESIVE CONDUCT. ELECTRODE?

NEOMED NON GEL-R TOTAL ADHESIVE CONDUCT. ELECTRODE is a medical device that received FDA 510(k) clearance on 1986-09-12. The listed applicant is Richards Medical Co., Inc.. The 510(k) number is K863360.

When did NEOMED NON GEL-R TOTAL ADHESIVE CONDUCT. ELECTRODE receive FDA 510(k) clearance?

NEOMED NON GEL-R TOTAL ADHESIVE CONDUCT. ELECTRODE received FDA 510(k) clearance on 1986-09-12, under 510(k) number K863360.

Who is the listed applicant for NEOMED NON GEL-R TOTAL ADHESIVE CONDUCT. ELECTRODE?

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

What is the FDA product code for NEOMED NON GEL-R TOTAL ADHESIVE CONDUCT. ELECTRODE?

The FDA product code for NEOMED NON GEL-R TOTAL ADHESIVE CONDUCT. ELECTRODE is GEI.

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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.