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FDA 510(k)

DAUM-LECTRIC MRI DRILLING MACHINE

K-Number: K021098 · 2002-12-03

Decision Date2002-12-03
Product CodeERL
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

DAUM-LECTRIC MRI DRILLING MACHINE is the device name listed in this FDA 510(k) record. The listed applicant is Mri Devices Daum GmbH. It received FDA 510(k) clearance on 2002-12-03 under 510(k) number K021098. The device is classified under product code ERL. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DAUM-LECTRIC MRI DRILLING MACHINE?

DAUM-LECTRIC MRI DRILLING MACHINE is a medical device that received FDA 510(k) clearance on 2002-12-03. The listed applicant is Mri Devices Daum GmbH. The 510(k) number is K021098.

When did DAUM-LECTRIC MRI DRILLING MACHINE receive FDA 510(k) clearance?

DAUM-LECTRIC MRI DRILLING MACHINE received FDA 510(k) clearance on 2002-12-03, under 510(k) number K021098.

Who is the listed applicant for DAUM-LECTRIC MRI DRILLING MACHINE?

The FDA 510(k) record lists Mri Devices Daum GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DAUM-LECTRIC MRI DRILLING MACHINE?

The FDA product code for DAUM-LECTRIC MRI DRILLING MACHINE is ERL.

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.

Related Devices (Code: ERL)

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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