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FDA 510(k)

RESTORE*

K-Number: K851929 · 1985-07-31

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1985-07-31
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

RESTORE* 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 1985-07-31 under 510(k) number K851929. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RESTORE*?

RESTORE* is a medical device that received FDA 510(k) clearance on 1985-07-31. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K851929.

When did RESTORE* receive FDA 510(k) clearance?

RESTORE* received FDA 510(k) clearance on 1985-07-31, under 510(k) number K851929.

Who is the listed applicant for RESTORE*?

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 RESTORE*?

The FDA product code for RESTORE* is EBF.

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Related Devices (Code: EBF)

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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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