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FDA 510(k)

CROWN & BRIDGE ALLOY

K-Number: K772256 · 1978-01-03

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1978-01-03
Product CodeEJH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CROWN & BRIDGE 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 1978-01-03 under 510(k) number K772256. The device is classified under product code EJH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CROWN & BRIDGE ALLOY?

CROWN & BRIDGE ALLOY is a medical device that received FDA 510(k) clearance on 1978-01-03. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K772256.

When did CROWN & BRIDGE ALLOY receive FDA 510(k) clearance?

CROWN & BRIDGE ALLOY received FDA 510(k) clearance on 1978-01-03, under 510(k) number K772256.

Who is the listed applicant for CROWN & BRIDGE 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 CROWN & BRIDGE ALLOY?

The FDA product code for CROWN & BRIDGE ALLOY is EJH.

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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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