FDA 510(k)

MBCP

K-Number: K051774 · 2006-01-20

Decision Date2006-01-20

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 2006-01-20 under 510(k) number K051774. 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 2006-01-20. The listed applicant is Biomatlante. The 510(k) number is K051774.

When did MBCP receive FDA 510(k) clearance?

MBCP received FDA 510(k) clearance on 2006-01-20, under 510(k) number K051774.

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.

K093122MBCP+K071121TRIBONE 80 K063527MBCP+K060732MBCP GEL K051885MBCP K043005MODIFICATION TO MBCP

View all 8 devices →

Related Devices (Code: MQV)

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.