FDA 510(k)

MBCP GEL

K-Number: K060732 · 2006-06-02

Decision Date2006-06-02

Product CodeLYC

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

MBCP GEL is the device name listed in this FDA 510(k) record. The listed applicant is Biomatlante. It received FDA 510(k) clearance on 2006-06-02 under 510(k) number K060732. The device is classified under product code LYC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MBCP GEL?

MBCP GEL is a medical device that received FDA 510(k) clearance on 2006-06-02. The listed applicant is Biomatlante. The 510(k) number is K060732.

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

MBCP GEL received FDA 510(k) clearance on 2006-06-02, under 510(k) number K060732.

Who is the listed applicant for MBCP GEL?

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 GEL?

The FDA product code for MBCP GEL is LYC.

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+K051774MBCP K051885MBCP K043005MODIFICATION TO MBCP

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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.