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FDA 510(k)

REPROCESSED DIAMOND BURS

K-Number: K041978 · 2004-11-23

ApplicantAlliance Medical Corp.
Decision Date2004-11-23
Product CodeNLN
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

REPROCESSED DIAMOND BURS is the device name listed in this FDA 510(k) record. The listed applicant is Alliance Medical Corp.. It received FDA 510(k) clearance on 2004-11-23 under 510(k) number K041978. The device is classified under product code NLN. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REPROCESSED DIAMOND BURS?

REPROCESSED DIAMOND BURS is a medical device that received FDA 510(k) clearance on 2004-11-23. The listed applicant is Alliance Medical Corp.. The 510(k) number is K041978.

When did REPROCESSED DIAMOND BURS receive FDA 510(k) clearance?

REPROCESSED DIAMOND BURS received FDA 510(k) clearance on 2004-11-23, under 510(k) number K041978.

Who is the listed applicant for REPROCESSED DIAMOND BURS?

The FDA 510(k) record lists Alliance Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REPROCESSED DIAMOND BURS?

The FDA product code for REPROCESSED DIAMOND BURS is NLN.

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Other records listing Alliance Medical Corp. 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.

K060648REPROCESSED PHACOEMULSIFICATION TIPSK061045REPROCESSED ELECTROPHYSIOLOGY CATHETERSK060049REPROCESSED COMPRESSION SLEEVESK060091ALLIANCE MEDICAL CORPORATION REPROCESSED COMPRESSION SLEEVESK053316REPROCESSED COMPRESSION SLEEVESK052918REPROCESSED EXTERNAL FIXATION DEVICES

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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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