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FDA 510(k)

CERAMCO PORCELAIN

K-Number: K803310 · 1981-01-14

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1981-01-14
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CERAMCO PORCELAIN 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 1981-01-14 under 510(k) number K803310. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CERAMCO PORCELAIN?

CERAMCO PORCELAIN is a medical device that received FDA 510(k) clearance on 1981-01-14. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K803310.

When did CERAMCO PORCELAIN receive FDA 510(k) clearance?

CERAMCO PORCELAIN received FDA 510(k) clearance on 1981-01-14, under 510(k) number K803310.

Who is the listed applicant for CERAMCO PORCELAIN?

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 CERAMCO PORCELAIN?

The FDA product code for CERAMCO PORCELAIN is EIH.

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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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