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FDA 510(k)

AUTO-VAC BIOPSY NEEDLE

K-Number: K912892 · 1992-02-07

ApplicantAngiomed GmbH & Co. Medizintechnik KG
Decision Date1992-02-07
Product CodeKNW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

AUTO-VAC BIOPSY NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Angiomed GmbH & Co. Medizintechnik KG. It received FDA 510(k) clearance on 1992-02-07 under 510(k) number K912892. 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 AUTO-VAC BIOPSY NEEDLE?

AUTO-VAC BIOPSY NEEDLE is a medical device that received FDA 510(k) clearance on 1992-02-07. The listed applicant is Angiomed GmbH & Co. Medizintechnik KG. The 510(k) number is K912892.

When did AUTO-VAC BIOPSY NEEDLE receive FDA 510(k) clearance?

AUTO-VAC BIOPSY NEEDLE received FDA 510(k) clearance on 1992-02-07, under 510(k) number K912892.

Who is the listed applicant for AUTO-VAC BIOPSY NEEDLE?

The FDA 510(k) record lists Angiomed GmbH & Co. Medizintechnik KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AUTO-VAC BIOPSY NEEDLE?

The FDA product code for AUTO-VAC BIOPSY NEEDLE is KNW.

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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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