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FDA 510(k)

SOYALA, SOYALA BLUE

K-Number: K060405 · 2006-06-21

ApplicantWeinmann Gerate Fur Medizin GmbH + Co. KG
Decision Date2006-06-21
Product CodeBZD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SOYALA, SOYALA BLUE 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 2006-06-21 under 510(k) number K060405. 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 SOYALA, SOYALA BLUE?

SOYALA, SOYALA BLUE is a medical device that received FDA 510(k) clearance on 2006-06-21. The listed applicant is Weinmann Gerate Fur Medizin GmbH + Co. KG. The 510(k) number is K060405.

When did SOYALA, SOYALA BLUE receive FDA 510(k) clearance?

SOYALA, SOYALA BLUE received FDA 510(k) clearance on 2006-06-21, under 510(k) number K060405.

Who is the listed applicant for SOYALA, SOYALA BLUE?

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 SOYALA, SOYALA BLUE?

The FDA product code for SOYALA, SOYALA BLUE is BZD.

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Other records listing Weinmann Gerate Fur Medizin GmbH + Co. KG as applicant

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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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