DAUM NEUROCUT NEUROBIOPSYNEEDLE
K-Number: K990278 · 1999-03-30
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Device Summary
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
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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