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FDA 510(k)

WEINMANNCOMFORT 2, MODEL WM 27600 AND WEINMANNAQUA, MODEL WM 27603

K-Number: K071163 · 2007-07-18

ApplicantWeinmann Gerate Fur Medizin GmbH + Co. KG
Decision Date2007-07-18
Product CodeBZD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

WEINMANNCOMFORT 2, MODEL WM 27600 AND WEINMANNAQUA, MODEL WM 27603 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 2007-07-18 under 510(k) number K071163. 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 WEINMANNCOMFORT 2, MODEL WM 27600 AND WEINMANNAQUA, MODEL WM 27603?

WEINMANNCOMFORT 2, MODEL WM 27600 AND WEINMANNAQUA, MODEL WM 27603 is a medical device that received FDA 510(k) clearance on 2007-07-18. The listed applicant is Weinmann Gerate Fur Medizin GmbH + Co. KG. The 510(k) number is K071163.

When did WEINMANNCOMFORT 2, MODEL WM 27600 AND WEINMANNAQUA, MODEL WM 27603 receive FDA 510(k) clearance?

WEINMANNCOMFORT 2, MODEL WM 27600 AND WEINMANNAQUA, MODEL WM 27603 received FDA 510(k) clearance on 2007-07-18, under 510(k) number K071163.

Who is the listed applicant for WEINMANNCOMFORT 2, MODEL WM 27600 AND WEINMANNAQUA, MODEL WM 27603?

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 WEINMANNCOMFORT 2, MODEL WM 27600 AND WEINMANNAQUA, MODEL WM 27603?

The FDA product code for WEINMANNCOMFORT 2, MODEL WM 27600 AND WEINMANNAQUA, MODEL WM 27603 is 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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