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FDA 510(k)

PALADUR

K-Number: K915898 · 1992-09-16

ApplicantHeraeus Kulzer, Inc.
Decision Date1992-09-16
Product CodeEBI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PALADUR is the device name listed in this FDA 510(k) record. The listed applicant is Heraeus Kulzer, Inc.. It received FDA 510(k) clearance on 1992-09-16 under 510(k) number K915898. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PALADUR?

PALADUR is a medical device that received FDA 510(k) clearance on 1992-09-16. The listed applicant is Heraeus Kulzer, Inc.. The 510(k) number is K915898.

When did PALADUR receive FDA 510(k) clearance?

PALADUR received FDA 510(k) clearance on 1992-09-16, under 510(k) number K915898.

Who is the listed applicant for PALADUR?

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

What is the FDA product code for PALADUR?

The FDA product code for PALADUR is EBI.

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Other records listing Heraeus Kulzer, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K091494FLEXITIME FLOWK063062HKBOND 2006K060994MONDIALK052543HERACERAM ZIRKONIAK043504PALAIMPACTK043295VERSYO.DIRECT

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Related Devices (Code: EBI)

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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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