AVALON GENERAL PURPOSE SCANNER, PREVIEW GP
K-Number: K904317 · 1991-02-13
Advertisement
Device Summary
Frequently Asked Questions
What is the AVALON GENERAL PURPOSE SCANNER, PREVIEW GP?
AVALON GENERAL PURPOSE SCANNER, PREVIEW GP is a medical device that received FDA 510(k) clearance on 1991-02-13. The listed applicant is Avalon Technology Corp.. The 510(k) number is K904317.
When did AVALON GENERAL PURPOSE SCANNER, PREVIEW GP receive FDA 510(k) clearance?
AVALON GENERAL PURPOSE SCANNER, PREVIEW GP received FDA 510(k) clearance on 1991-02-13, under 510(k) number K904317.
Who is the listed applicant for AVALON GENERAL PURPOSE SCANNER, PREVIEW GP?
The FDA 510(k) record lists Avalon Technology Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AVALON GENERAL PURPOSE SCANNER, PREVIEW GP?
The FDA product code for AVALON GENERAL PURPOSE SCANNER, PREVIEW GP is DPW.
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 Avalon Technology 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: DPW)
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