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FDA 510(k)

BETA-POWDER

K-Number: K063236 · 2007-02-16

ApplicantBrainbase Corporation
Decision Date2007-02-16
Product CodeKOJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BETA-POWDER is the device name listed in this FDA 510(k) record. The listed applicant is Brainbase Corporation. It received FDA 510(k) clearance on 2007-02-16 under 510(k) number K063236. The device is classified under product code KOJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BETA-POWDER?

BETA-POWDER is a medical device that received FDA 510(k) clearance on 2007-02-16. The listed applicant is Brainbase Corporation. The 510(k) number is K063236.

When did BETA-POWDER receive FDA 510(k) clearance?

BETA-POWDER received FDA 510(k) clearance on 2007-02-16, under 510(k) number K063236.

Who is the listed applicant for BETA-POWDER?

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

What is the FDA product code for BETA-POWDER?

The FDA product code for BETA-POWDER is KOJ.

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Other records listing Brainbase Corporation 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.

K083372ARROWBONE-A, ARROWBONE-BK052254MYTIS ARROW XXXX

Related Devices (Code: KOJ)

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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