FDA 510(k)

NEW BRID

K-Number: K041780 · 2004-08-11

ApplicantMedical Imaging Solutions, Inc.

Decision Date2004-08-11

Product CodeOWB

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

NEW BRID is the device name listed in this FDA 510(k) record. The listed applicant is Medical Imaging Solutions, Inc.. It received FDA 510(k) clearance on 2004-08-11 under 510(k) number K041780. The device is classified under product code OWB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEW BRID?

NEW BRID is a medical device that received FDA 510(k) clearance on 2004-08-11. The listed applicant is Medical Imaging Solutions, Inc.. The 510(k) number is K041780.

When did NEW BRID receive FDA 510(k) clearance?

NEW BRID received FDA 510(k) clearance on 2004-08-11, under 510(k) number K041780.

Who is the listed applicant for NEW BRID?

The FDA 510(k) record lists Medical Imaging Solutions, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEW BRID?

The FDA product code for NEW BRID is OWB.

Related Devices (Code: OWB)

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.

K253726uAngio AVIVA CXShanghai United Imaging Healthcare Co., Ltd.K261413EXTRON 3;EXTRON 6DRTECH Corporation K254205Zenition 30Philips Medical Systems Nederland B.V.K260607Shield System (Siemens 30x40)Radiaction , Ltd.K253670SmartCT (R3.0 (L10))Philips Medical Systems B.V.K252735C-beamPulmera, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.