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FDA 510(k)

MODIFICATION TO MBCP

K-Number: K043005 · 2005-05-03

ApplicantBiomatlante
Decision Date2005-05-03
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO MBCP is the device name listed in this FDA 510(k) record. The listed applicant is Biomatlante. It received FDA 510(k) clearance on 2005-05-03 under 510(k) number K043005. 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 MODIFICATION TO MBCP?

MODIFICATION TO MBCP is a medical device that received FDA 510(k) clearance on 2005-05-03. The listed applicant is Biomatlante. The 510(k) number is K043005.

When did MODIFICATION TO MBCP receive FDA 510(k) clearance?

MODIFICATION TO MBCP received FDA 510(k) clearance on 2005-05-03, under 510(k) number K043005.

Who is the listed applicant for MODIFICATION TO 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 MODIFICATION TO MBCP?

The FDA product code for MODIFICATION TO MBCP is MQV.

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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.

K093122MBCP+K071121TRIBONE 80K063527MBCP+K060732MBCP GELK051774MBCPK051885MBCP

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Related Devices (Code: MQV)

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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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