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FDA 510(k)

DAUM DOUBLE-SHOOT BISOPSY GUN

K-Number: K010037 · 2001-03-22

ApplicantDaum GmbH
Decision Date2001-03-22
Product CodeKNW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DAUM DOUBLE-SHOOT BISOPSY GUN is the device name listed in this FDA 510(k) record. The listed applicant is Daum GmbH. It received FDA 510(k) clearance on 2001-03-22 under 510(k) number K010037. 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 DOUBLE-SHOOT BISOPSY GUN?

DAUM DOUBLE-SHOOT BISOPSY GUN is a medical device that received FDA 510(k) clearance on 2001-03-22. The listed applicant is Daum GmbH. The 510(k) number is K010037.

When did DAUM DOUBLE-SHOOT BISOPSY GUN receive FDA 510(k) clearance?

DAUM DOUBLE-SHOOT BISOPSY GUN received FDA 510(k) clearance on 2001-03-22, under 510(k) number K010037.

Who is the listed applicant for DAUM DOUBLE-SHOOT BISOPSY GUN?

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 DOUBLE-SHOOT BISOPSY GUN?

The FDA product code for DAUM DOUBLE-SHOOT BISOPSY GUN is KNW.

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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.

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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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