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FDA 510(k)

PROCEARA COPINGS AND PONTIC

K-Number: K032562 · 2004-02-06

ApplicantNobel Biocare AB
Decision Date2004-02-06
Product CodeELL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PROCEARA COPINGS AND PONTIC is the device name listed in this FDA 510(k) record. The listed applicant is Nobel Biocare AB. It received FDA 510(k) clearance on 2004-02-06 under 510(k) number K032562. 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 PROCEARA COPINGS AND PONTIC?

PROCEARA COPINGS AND PONTIC is a medical device that received FDA 510(k) clearance on 2004-02-06. The listed applicant is Nobel Biocare AB. The 510(k) number is K032562.

When did PROCEARA COPINGS AND PONTIC receive FDA 510(k) clearance?

PROCEARA COPINGS AND PONTIC received FDA 510(k) clearance on 2004-02-06, under 510(k) number K032562.

Who is the listed applicant for PROCEARA COPINGS AND PONTIC?

The FDA 510(k) record lists Nobel Biocare AB as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PROCEARA COPINGS AND PONTIC?

The FDA product code for PROCEARA COPINGS AND PONTIC is 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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