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FDA 510(k)

TOOTHBRUSH, REACH

K-Number: K770749 · 1977-06-20

Decision Date1977-06-20
Product CodeEFW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TOOTHBRUSH, REACH is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Professionals, Inc.. It received FDA 510(k) clearance on 1977-06-20 under 510(k) number K770749. 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 TOOTHBRUSH, REACH?

TOOTHBRUSH, REACH is a medical device that received FDA 510(k) clearance on 1977-06-20. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K770749.

When did TOOTHBRUSH, REACH receive FDA 510(k) clearance?

TOOTHBRUSH, REACH received FDA 510(k) clearance on 1977-06-20, under 510(k) number K770749.

Who is the listed applicant for TOOTHBRUSH, REACH?

The FDA 510(k) record lists Johnson & Johnson Professionals, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TOOTHBRUSH, REACH?

The FDA product code for TOOTHBRUSH, REACH 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 Johnson & Johnson Professionals, 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.

View all 206 devices →

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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