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FDA 510(k)

DAUM NEUROCUT NEUROBIOPSYNEEDLE

K-Number: K990278 · 1999-03-30

ApplicantDaum Corp.
Decision Date1999-03-30
Product CodeKNW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DAUM NEUROCUT NEUROBIOPSYNEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Daum Corp.. It received FDA 510(k) clearance on 1999-03-30 under 510(k) number K990278. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DAUM NEUROCUT NEUROBIOPSYNEEDLE?

DAUM NEUROCUT NEUROBIOPSYNEEDLE is a medical device that received FDA 510(k) clearance on 1999-03-30. The listed applicant is Daum Corp.. The 510(k) number is K990278.

When did DAUM NEUROCUT NEUROBIOPSYNEEDLE receive FDA 510(k) clearance?

DAUM NEUROCUT NEUROBIOPSYNEEDLE received FDA 510(k) clearance on 1999-03-30, under 510(k) number K990278.

Who is the listed applicant for DAUM NEUROCUT NEUROBIOPSYNEEDLE?

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

What is the FDA product code for DAUM NEUROCUT NEUROBIOPSYNEEDLE?

The FDA product code for DAUM NEUROCUT NEUROBIOPSYNEEDLE is KNW.

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 Daum 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.

Related Devices (Code: KNW)

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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