EZER, Portable X-ray System
K-Number: K190935 · 2019-12-19
Device Summary
Frequently Asked Questions
What is the EZER, Portable X-ray System?
EZER, Portable X-ray System is a medical device that received FDA 510(k) clearance on 2019-12-19. The listed applicant is Livermoretech, Inc.. The 510(k) number is K190935.
When did EZER, Portable X-ray System receive FDA 510(k) clearance?
EZER, Portable X-ray System received FDA 510(k) clearance on 2019-12-19, under 510(k) number K190935.
Who is the listed applicant for EZER, Portable X-ray System?
The FDA 510(k) record lists Livermoretech, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EZER, Portable X-ray System?
The FDA product code for EZER, Portable X-ray System is EHD.
Other records listing Livermoretech, 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: EHD)
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.