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FDA 510(k)

MARROW PLUS (M+)

K-Number: K051695 · 2005-07-19

ApplicantBerkeley Advanced Biomaterials, Inc.
Decision Date2005-07-19
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MARROW PLUS (M+) is the device name listed in this FDA 510(k) record. The listed applicant is Berkeley Advanced Biomaterials, Inc.. It received FDA 510(k) clearance on 2005-07-19 under 510(k) number K051695. 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 MARROW PLUS (M+)?

MARROW PLUS (M+) is a medical device that received FDA 510(k) clearance on 2005-07-19. The listed applicant is Berkeley Advanced Biomaterials, Inc.. The 510(k) number is K051695.

When did MARROW PLUS (M+) receive FDA 510(k) clearance?

MARROW PLUS (M+) received FDA 510(k) clearance on 2005-07-19, under 510(k) number K051695.

Who is the listed applicant for MARROW PLUS (M+)?

The FDA 510(k) record lists Berkeley Advanced Biomaterials, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MARROW PLUS (M+)?

The FDA product code for MARROW PLUS (M+) is 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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