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FDA 510(k)

LIFEBRIDGE B2T, MODEL 7001

K-Number: K090006 · 2009-10-15

ApplicantLifebridge Medizintechnik AG
Decision Date2009-10-15
Product CodeDTQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LIFEBRIDGE B2T, MODEL 7001 is the device name listed in this FDA 510(k) record. The listed applicant is Lifebridge Medizintechnik AG. It received FDA 510(k) clearance on 2009-10-15 under 510(k) number K090006. The device is classified under product code DTQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIFEBRIDGE B2T, MODEL 7001?

LIFEBRIDGE B2T, MODEL 7001 is a medical device that received FDA 510(k) clearance on 2009-10-15. The listed applicant is Lifebridge Medizintechnik AG. The 510(k) number is K090006.

When did LIFEBRIDGE B2T, MODEL 7001 receive FDA 510(k) clearance?

LIFEBRIDGE B2T, MODEL 7001 received FDA 510(k) clearance on 2009-10-15, under 510(k) number K090006.

Who is the listed applicant for LIFEBRIDGE B2T, MODEL 7001?

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

What is the FDA product code for LIFEBRIDGE B2T, MODEL 7001?

The FDA product code for LIFEBRIDGE B2T, MODEL 7001 is DTQ.

Related Clinical Trials

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Other records listing Lifebridge Medizintechnik AG as applicant

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.

K111384LIFEBRIDGEK103357LIFEBRIDGE

Related Devices (Code: DTQ)

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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