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FDA 510(k)

ALTIS (RESIN, CROWN AND BRIDGES)

K-Number: K902040 · 1990-10-09

ApplicantPb2 Investment, Inc.
Decision Date1990-10-09
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ALTIS (RESIN, CROWN AND BRIDGES) is the device name listed in this FDA 510(k) record. The listed applicant is Pb2 Investment, Inc.. It received FDA 510(k) clearance on 1990-10-09 under 510(k) number K902040. 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 ALTIS (RESIN, CROWN AND BRIDGES)?

ALTIS (RESIN, CROWN AND BRIDGES) is a medical device that received FDA 510(k) clearance on 1990-10-09. The listed applicant is Pb2 Investment, Inc.. The 510(k) number is K902040.

When did ALTIS (RESIN, CROWN AND BRIDGES) receive FDA 510(k) clearance?

ALTIS (RESIN, CROWN AND BRIDGES) received FDA 510(k) clearance on 1990-10-09, under 510(k) number K902040.

Who is the listed applicant for ALTIS (RESIN, CROWN AND BRIDGES)?

The FDA 510(k) record lists Pb2 Investment, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ALTIS (RESIN, CROWN AND BRIDGES)?

The FDA product code for ALTIS (RESIN, CROWN AND BRIDGES) is EBF.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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