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FDA 510(k)

MBCP+

K-Number: K063527 · 2007-07-30

ApplicantBiomatlante
Decision Date2007-07-30
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MBCP+ is the device name listed in this FDA 510(k) record. The listed applicant is Biomatlante. It received FDA 510(k) clearance on 2007-07-30 under 510(k) number K063527. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MBCP+?

MBCP+ is a medical device that received FDA 510(k) clearance on 2007-07-30. The listed applicant is Biomatlante. The 510(k) number is K063527.

When did MBCP+ receive FDA 510(k) clearance?

MBCP+ received FDA 510(k) clearance on 2007-07-30, under 510(k) number K063527.

Who is the listed applicant for MBCP+?

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

What is the FDA product code for MBCP+?

The FDA product code for MBCP+ is MQV.

Other records listing Biomatlante 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.

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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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