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FDA 510(k)

PORTABLE TOOTHBRUSH KIT (NO SAMPLE)

K-Number: K812361 · 1981-11-20

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

Device Summary

PORTABLE TOOTHBRUSH KIT (NO SAMPLE) 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 K812361. 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 PORTABLE TOOTHBRUSH KIT (NO SAMPLE)?

PORTABLE TOOTHBRUSH KIT (NO SAMPLE) 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 K812361.

When did PORTABLE TOOTHBRUSH KIT (NO SAMPLE) receive FDA 510(k) clearance?

PORTABLE TOOTHBRUSH KIT (NO SAMPLE) received FDA 510(k) clearance on 1981-11-20, under 510(k) number K812361.

Who is the listed applicant for PORTABLE TOOTHBRUSH KIT (NO SAMPLE)?

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 PORTABLE TOOTHBRUSH KIT (NO SAMPLE)?

The FDA product code for PORTABLE TOOTHBRUSH KIT (NO SAMPLE) 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

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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