ALT QVET
K-Number: K944080 · 1994-11-22
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Device Summary
Frequently Asked Questions
What is the ALT QVET?
ALT QVET is a medical device that received FDA 510(k) clearance on 1994-11-22. The listed applicant is Prisma Systems. The 510(k) number is K944080.
When did ALT QVET receive FDA 510(k) clearance?
ALT QVET received FDA 510(k) clearance on 1994-11-22, under 510(k) number K944080.
Who is the listed applicant for ALT QVET?
The FDA 510(k) record lists Prisma Systems as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ALT QVET?
The FDA product code for ALT QVET is CKA.
Other records listing Prisma Systems 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: CKA)
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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