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FDA 510(k)

VALULINE* AMALGAM ALLOY

K-Number: K821971 · 1982-07-20

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1982-07-20
Product CodeEJJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VALULINE* AMALGAM ALLOY 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 1982-07-20 under 510(k) number K821971. The device is classified under product code EJJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VALULINE* AMALGAM ALLOY?

VALULINE* AMALGAM ALLOY is a medical device that received FDA 510(k) clearance on 1982-07-20. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K821971.

When did VALULINE* AMALGAM ALLOY receive FDA 510(k) clearance?

VALULINE* AMALGAM ALLOY received FDA 510(k) clearance on 1982-07-20, under 510(k) number K821971.

Who is the listed applicant for VALULINE* AMALGAM ALLOY?

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 VALULINE* AMALGAM ALLOY?

The FDA product code for VALULINE* AMALGAM ALLOY is EJJ.

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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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