DRX-REVOLUTION MOBILE X-RAY SYSTEM
K-Number: K120062 · 2012-04-13
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Device Summary
Frequently Asked Questions
What is the DRX-REVOLUTION MOBILE X-RAY SYSTEM?
DRX-REVOLUTION MOBILE X-RAY SYSTEM is a medical device that received FDA 510(k) clearance on 2012-04-13. The listed applicant is Carestream Health, Inc.. The 510(k) number is K120062.
When did DRX-REVOLUTION MOBILE X-RAY SYSTEM receive FDA 510(k) clearance?
DRX-REVOLUTION MOBILE X-RAY SYSTEM received FDA 510(k) clearance on 2012-04-13, under 510(k) number K120062.
Who is the listed applicant for DRX-REVOLUTION MOBILE X-RAY SYSTEM?
The FDA 510(k) record lists Carestream Health, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DRX-REVOLUTION MOBILE X-RAY SYSTEM?
The FDA product code for DRX-REVOLUTION MOBILE X-RAY SYSTEM is IZL.
Related Clinical Trials
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.
Other records listing Carestream Health, 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.
Related Devices (Code: IZL)
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.
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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