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FDA 510(k)

DIGIVIEW 250

K-Number: K103348 · 2011-10-20

ApplicantKub Technologies, Inc.
Decision Date2011-10-20
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIGIVIEW 250 is the device name listed in this FDA 510(k) record. The listed applicant is Kub Technologies, Inc.. It received FDA 510(k) clearance on 2011-10-20 under 510(k) number K103348. 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 DIGIVIEW 250?

DIGIVIEW 250 is a medical device that received FDA 510(k) clearance on 2011-10-20. The listed applicant is Kub Technologies, Inc.. The 510(k) number is K103348.

When did DIGIVIEW 250 receive FDA 510(k) clearance?

DIGIVIEW 250 received FDA 510(k) clearance on 2011-10-20, under 510(k) number K103348.

Who is the listed applicant for DIGIVIEW 250?

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

What is the FDA product code for DIGIVIEW 250?

The FDA product code for DIGIVIEW 250 is MQB.

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Other records listing Kub Technologies, Inc. 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.

K210955Kubtec Mozart Supra (XPERT 84) Radiography SystemK210956Kubtec Mozart (XPERT42)K210957Kubec Xpert 80 Radiography SystemK200756Kubtec Mozart SupraK183624Kubtec Mozart (Xpert42)K083510KUBTEC XPERT 20

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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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