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FDA 510(k)

DRAEGER MEDICAL INFORMATION BUS (MIB, MIB II, MIB DUO) PROTOCOL CONVERTERS

K-Number: K050974 · 2005-04-29

ApplicantDraeger Medical Systems, Inc.
Decision Date2005-04-29
Product CodeDRQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DRAEGER MEDICAL INFORMATION BUS (MIB, MIB II, MIB DUO) PROTOCOL CONVERTERS is the device name listed in this FDA 510(k) record. The listed applicant is Draeger Medical Systems, Inc.. It received FDA 510(k) clearance on 2005-04-29 under 510(k) number K050974. The device is classified under product code DRQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DRAEGER MEDICAL INFORMATION BUS (MIB, MIB II, MIB DUO) PROTOCOL CONVERTERS?

DRAEGER MEDICAL INFORMATION BUS (MIB, MIB II, MIB DUO) PROTOCOL CONVERTERS is a medical device that received FDA 510(k) clearance on 2005-04-29. The listed applicant is Draeger Medical Systems, Inc.. The 510(k) number is K050974.

When did DRAEGER MEDICAL INFORMATION BUS (MIB, MIB II, MIB DUO) PROTOCOL CONVERTERS receive FDA 510(k) clearance?

DRAEGER MEDICAL INFORMATION BUS (MIB, MIB II, MIB DUO) PROTOCOL CONVERTERS received FDA 510(k) clearance on 2005-04-29, under 510(k) number K050974.

Who is the listed applicant for DRAEGER MEDICAL INFORMATION BUS (MIB, MIB II, MIB DUO) PROTOCOL CONVERTERS?

The FDA 510(k) record lists Draeger Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DRAEGER MEDICAL INFORMATION BUS (MIB, MIB II, MIB DUO) PROTOCOL CONVERTERS?

The FDA product code for DRAEGER MEDICAL INFORMATION BUS (MIB, MIB II, MIB DUO) PROTOCOL CONVERTERS is DRQ.

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Other records listing Draeger Medical Systems, Inc. as applicant

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Related Devices (Code: DRQ)

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.

K172216ACIST RXi Mini SystemAcist Medical Systems, Inc.K050006BOREALIS AMPLIFIER (CLEARSIGN), MODEL 2001232 160 CHANNEL VERSION, 2001267 80 CHANNEL VERSION, 2001268 40 CHANNEL VERSIOC.R. Bard, Inc.K033807INFINITYEDICAL INFORMATION BUS (MIB/MIB II AND MIB DUO) PROTOCOL CONVERTERDraeger Medical Systems, Inc.K013205MILLAR PRESSURE CONTROL UNIT MODEL PCU-2000Millar Instruments, Inc.K020277SIEMENS MEDICAL INFROMATION BUS (MIB II) PROTOCOL CONVERTERSiemens Medical Solutions USA, Inc.K010640SIEMENS MEDICAL INFORMATION BUS (MIB II) PROTOCOL CONVERTERSiemens Medical Solutions USA, Inc.

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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