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FDA 510(k)

PORT. TOOTHBRUSH KIT W/4 G. TOOTHPASTE

K-Number: K812364 · 1981-11-20

Decision Date1981-11-20
Product CodeEFW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PORT. TOOTHBRUSH KIT W/4 G. TOOTHPASTE is the device name listed in this FDA 510(k) record. The listed applicant is Jdm Commodities. It received FDA 510(k) clearance on 1981-11-20 under 510(k) number K812364. The device is classified under product code EFW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PORT. TOOTHBRUSH KIT W/4 G. TOOTHPASTE?

PORT. TOOTHBRUSH KIT W/4 G. TOOTHPASTE is a medical device that received FDA 510(k) clearance on 1981-11-20. The listed applicant is Jdm Commodities. The 510(k) number is K812364.

When did PORT. TOOTHBRUSH KIT W/4 G. TOOTHPASTE receive FDA 510(k) clearance?

PORT. TOOTHBRUSH KIT W/4 G. TOOTHPASTE received FDA 510(k) clearance on 1981-11-20, under 510(k) number K812364.

Who is the listed applicant for PORT. TOOTHBRUSH KIT W/4 G. TOOTHPASTE?

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

What is the FDA product code for PORT. TOOTHBRUSH KIT W/4 G. TOOTHPASTE?

The FDA product code for PORT. TOOTHBRUSH KIT W/4 G. TOOTHPASTE is EFW.

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.

Other records listing Jdm Commodities 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.

Related Devices (Code: EFW)

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.

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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