CLEARVISION DR 7000F— 510(k) K102327

Substantially Equivalent

Jpi Healthcare Co, Ltd.

FDA 510(k) clearance K102327 for CLEARVISION DR 7000F, Substantially Equivalent on 2012-04-13. Applicant: Jpi Healthcare Co, Ltd.. Device class: 2.

Clearance details

Applicant: Jpi Healthcare Co, Ltd.
Product code: Code MQB
Device class: Class 2
Regulation: 21 CFR 892.1680
Advisory panel: Radiology
Date received: 2010-08-17
Decision date: 2012-04-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Seoul, KR

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.