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FDA 510(k)

WEINMANNCOMPACT, MODEL WM 27380; WEINMANNCLICK2, MODEL WM 27340

K-Number: K072009 · 2007-12-14

ApplicantWeinmann Gerate Fur Medizin GmbH + Co. KG
Decision Date2007-12-14
Product CodeBZD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

WEINMANNCOMPACT, MODEL WM 27380; WEINMANNCLICK2, MODEL WM 27340 is the device name listed in this FDA 510(k) record. The listed applicant is Weinmann Gerate Fur Medizin GmbH + Co. KG. It received FDA 510(k) clearance on 2007-12-14 under 510(k) number K072009. The device is classified under product code BZD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WEINMANNCOMPACT, MODEL WM 27380; WEINMANNCLICK2, MODEL WM 27340?

WEINMANNCOMPACT, MODEL WM 27380; WEINMANNCLICK2, MODEL WM 27340 is a medical device that received FDA 510(k) clearance on 2007-12-14. The listed applicant is Weinmann Gerate Fur Medizin GmbH + Co. KG. The 510(k) number is K072009.

When did WEINMANNCOMPACT, MODEL WM 27380; WEINMANNCLICK2, MODEL WM 27340 receive FDA 510(k) clearance?

WEINMANNCOMPACT, MODEL WM 27380; WEINMANNCLICK2, MODEL WM 27340 received FDA 510(k) clearance on 2007-12-14, under 510(k) number K072009.

Who is the listed applicant for WEINMANNCOMPACT, MODEL WM 27380; WEINMANNCLICK2, MODEL WM 27340?

The FDA 510(k) record lists Weinmann Gerate Fur Medizin GmbH + Co. KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WEINMANNCOMPACT, MODEL WM 27380; WEINMANNCLICK2, MODEL WM 27340?

The FDA product code for WEINMANNCOMPACT, MODEL WM 27380; WEINMANNCLICK2, MODEL WM 27340 is BZD.

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Related Devices (Code: BZD)

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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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