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FDA 510(k)

PROCERAM PORCELAIN

K-Number: K903907 · 1990-11-09

ApplicantNobelpharma USA, Inc.
Decision Date1990-11-09
Product CodeELL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PROCERAM PORCELAIN is the device name listed in this FDA 510(k) record. The listed applicant is Nobelpharma USA, Inc.. It received FDA 510(k) clearance on 1990-11-09 under 510(k) number K903907. The device is classified under product code ELL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROCERAM PORCELAIN?

PROCERAM PORCELAIN is a medical device that received FDA 510(k) clearance on 1990-11-09. The listed applicant is Nobelpharma USA, Inc.. The 510(k) number is K903907.

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

PROCERAM PORCELAIN received FDA 510(k) clearance on 1990-11-09, under 510(k) number K903907.

Who is the listed applicant for PROCERAM PORCELAIN?

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

What is the FDA product code for PROCERAM PORCELAIN?

The FDA product code for PROCERAM PORCELAIN is ELL.

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Other records listing Nobelpharma USA, Inc. as applicant

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Related Devices (Code: ELL)

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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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