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FDA 510(k)

CLEARVISION DR 7000F

K-Number: K102327 · 2012-04-13

ApplicantJpi Healthcare Co, Ltd.
Decision Date2012-04-13
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CLEARVISION DR 7000F is the device name listed in this FDA 510(k) record. The listed applicant is Jpi Healthcare Co, Ltd.. It received FDA 510(k) clearance on 2012-04-13 under 510(k) number K102327. 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 CLEARVISION DR 7000F?

CLEARVISION DR 7000F is a medical device that received FDA 510(k) clearance on 2012-04-13. The listed applicant is Jpi Healthcare Co, Ltd.. The 510(k) number is K102327.

When did CLEARVISION DR 7000F receive FDA 510(k) clearance?

CLEARVISION DR 7000F received FDA 510(k) clearance on 2012-04-13, under 510(k) number K102327.

Who is the listed applicant for CLEARVISION DR 7000F?

The FDA 510(k) record lists Jpi Healthcare Co, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CLEARVISION DR 7000F?

The FDA product code for CLEARVISION DR 7000F is MQB.

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Other records listing Jpi Healthcare Co, Ltd. 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.

K260482DRE DuoK244010ExamVue ApexK213057ExamVue DuoK101779CLEARVISION DR 2000 DIGITAL RADIOGRAPHY X-RAY SYSTEMK955706JPI AUTOMATIC X-RAY FILM PROCESSORK954161JPI INTENSIFYING SCREEN

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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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