PIXX 1717; PIXX 1417; PIXX 1212; Digital Diagnostic X-ray Receptor Panels
K-Number: K180976 · 2018-05-24
Device Summary
Frequently Asked Questions
What is the PIXX 1717; PIXX 1417; PIXX 1212; Digital Diagnostic X-ray Receptor Panels?
PIXX 1717; PIXX 1417; PIXX 1212; Digital Diagnostic X-ray Receptor Panels is a medical device that received FDA 510(k) clearance on 2018-05-24. The listed applicant is Pixxgen Corporation. The 510(k) number is K180976.
When did PIXX 1717; PIXX 1417; PIXX 1212; Digital Diagnostic X-ray Receptor Panels receive FDA 510(k) clearance?
PIXX 1717; PIXX 1417; PIXX 1212; Digital Diagnostic X-ray Receptor Panels received FDA 510(k) clearance on 2018-05-24, under 510(k) number K180976.
Who is the listed applicant for PIXX 1717; PIXX 1417; PIXX 1212; Digital Diagnostic X-ray Receptor Panels?
The FDA 510(k) record lists Pixxgen Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PIXX 1717; PIXX 1417; PIXX 1212; Digital Diagnostic X-ray Receptor Panels?
The FDA product code for PIXX 1717; PIXX 1417; PIXX 1212; Digital Diagnostic X-ray Receptor Panels is MQB.
Other records listing Pixxgen Corporation 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: 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.
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.