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FDA 510(k)

MOBIVISION

K-Number: K100001 · 2010-06-25

ApplicantAlmana Medical Imaging
Decision Date2010-06-25
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MOBIVISION is the device name listed in this FDA 510(k) record. The listed applicant is Almana Medical Imaging. It received FDA 510(k) clearance on 2010-06-25 under 510(k) number K100001. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOBIVISION?

MOBIVISION is a medical device that received FDA 510(k) clearance on 2010-06-25. The listed applicant is Almana Medical Imaging. The 510(k) number is K100001.

When did MOBIVISION receive FDA 510(k) clearance?

MOBIVISION received FDA 510(k) clearance on 2010-06-25, under 510(k) number K100001.

Who is the listed applicant for MOBIVISION?

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

What is the FDA product code for MOBIVISION?

The FDA product code for MOBIVISION is MQB.

Related Clinical Trials

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Other records listing Almana Medical Imaging 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.

K082064RADVISION ET DIAGNOSTIC X-RAY SYSTEMK080847RFVISION, MODEL 9.9DK080614DR VISION NEO, DR VISION DOUK072659RAD VISION, MODELS E AND EU

Related Devices (Code: MQB)

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.

K2538000909FCE, 0909FCE-HSRayence Co., Ltd.K260820VIVIX-S 4386W (FXRD-4386WA)Vieworks Co., Ltd.K252996Universal 1417PIKonica Minolta Healthcare Americas, Inc.K252911Lux HD 2530 detector (Lux HD 2530)Iray Imaging Technology (Haining) LimitedK250211Yushan X-Ray Flat Panel DetectorInnocare Optoelectronics Corp.K250665SKR 3000Konica Minolta, Inc.

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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