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FDA 510(k)

BINDER CO2 INCUBATOR SERIE CB

K-Number: K032526 · 2003-08-29

ApplicantBinder GmbH
Decision Date2003-08-29
Product CodeMQG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

BINDER CO2 INCUBATOR SERIE CB is the device name listed in this FDA 510(k) record. The listed applicant is Binder GmbH. It received FDA 510(k) clearance on 2003-08-29 under 510(k) number K032526. The device is classified under product code MQG. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BINDER CO2 INCUBATOR SERIE CB?

BINDER CO2 INCUBATOR SERIE CB is a medical device that received FDA 510(k) clearance on 2003-08-29. The listed applicant is Binder GmbH. The 510(k) number is K032526.

When did BINDER CO2 INCUBATOR SERIE CB receive FDA 510(k) clearance?

BINDER CO2 INCUBATOR SERIE CB received FDA 510(k) clearance on 2003-08-29, under 510(k) number K032526.

Who is the listed applicant for BINDER CO2 INCUBATOR SERIE CB?

The FDA 510(k) record lists Binder GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BINDER CO2 INCUBATOR SERIE CB?

The FDA product code for BINDER CO2 INCUBATOR SERIE CB is MQG.

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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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