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FDA 510(k)

DIMENSION PENTA H, DIMENSION PENTA H QUICK

K-Number: K000591 · 2000-03-30

Decision Date2000-03-30
Product CodeELW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DIMENSION PENTA H, DIMENSION PENTA H QUICK is the device name listed in this FDA 510(k) record. The listed applicant is Espe Dental AG. It received FDA 510(k) clearance on 2000-03-30 under 510(k) number K000591. The device is classified under product code ELW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIMENSION PENTA H, DIMENSION PENTA H QUICK?

DIMENSION PENTA H, DIMENSION PENTA H QUICK is a medical device that received FDA 510(k) clearance on 2000-03-30. The listed applicant is Espe Dental AG. The 510(k) number is K000591.

When did DIMENSION PENTA H, DIMENSION PENTA H QUICK receive FDA 510(k) clearance?

DIMENSION PENTA H, DIMENSION PENTA H QUICK received FDA 510(k) clearance on 2000-03-30, under 510(k) number K000591.

Who is the listed applicant for DIMENSION PENTA H, DIMENSION PENTA H QUICK?

The FDA 510(k) record lists Espe Dental AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIMENSION PENTA H, DIMENSION PENTA H QUICK?

The FDA product code for DIMENSION PENTA H, DIMENSION PENTA H QUICK is ELW.

Related Clinical Trials

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.

Other records listing Espe Dental AG 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.

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Related Devices (Code: ELW)

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.

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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