CFX 625
K-Number: K883976 · 1988-12-13
Advertisement
Device Summary
Frequently Asked Questions
What is the CFX 625?
CFX 625 is a medical device that received FDA 510(k) clearance on 1988-12-13. The listed applicant is Fischer Imaging Corp.. The 510(k) number is K883976.
When did CFX 625 receive FDA 510(k) clearance?
CFX 625 received FDA 510(k) clearance on 1988-12-13, under 510(k) number K883976.
Who is the listed applicant for CFX 625?
The FDA 510(k) record lists Fischer Imaging Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CFX 625?
The FDA product code for CFX 625 is IZO.
Other records listing Fischer Imaging Corp. 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: IZO)
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.
Advertisement