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FDA 510(k)

DAUM BIOPSYGUN

K-Number: K974576 · 1998-03-06

ApplicantDaum Corp.
Decision Date1998-03-06
Product CodeKNW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DAUM BIOPSYGUN is the device name listed in this FDA 510(k) record. The listed applicant is Daum Corp.. It received FDA 510(k) clearance on 1998-03-06 under 510(k) number K974576. 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 BIOPSYGUN?

DAUM BIOPSYGUN is a medical device that received FDA 510(k) clearance on 1998-03-06. The listed applicant is Daum Corp.. The 510(k) number is K974576.

When did DAUM BIOPSYGUN receive FDA 510(k) clearance?

DAUM BIOPSYGUN received FDA 510(k) clearance on 1998-03-06, under 510(k) number K974576.

Who is the listed applicant for DAUM BIOPSYGUN?

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 BIOPSYGUN?

The FDA product code for DAUM BIOPSYGUN is KNW.

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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.

K990278DAUM NEUROCUT NEUROBIOPSYNEEDLEK981320DAUM BONE BIOPSY SETK974631DAUM NEUROBIOPSY NEEDLEK974575DAUM ASPIRATIONBIOPSY NEEDLEK974574DAUM NEUROPUNCTURE NEEDLE

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.

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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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