DAUM NEUROGATE TROCAR
K-Number: K990782 · 1999-04-28
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Device Summary
Frequently Asked Questions
What is the DAUM NEUROGATE TROCAR?
DAUM NEUROGATE TROCAR is a medical device that received FDA 510(k) clearance on 1999-04-28. The listed applicant is Daum GmbH. The 510(k) number is K990782.
When did DAUM NEUROGATE TROCAR receive FDA 510(k) clearance?
DAUM NEUROGATE TROCAR received FDA 510(k) clearance on 1999-04-28, under 510(k) number K990782.
Who is the listed applicant for DAUM NEUROGATE TROCAR?
The FDA 510(k) record lists Daum GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DAUM NEUROGATE TROCAR?
The FDA product code for DAUM NEUROGATE TROCAR 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 GmbH 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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