Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K943042Substantially Equivalent

Bun Qvet

Prisma Systems, Rome NY / Traditional, Substantially Equivalent

K943042 is the FDA 510(k) clearance record for BUN QVET, a class II device, cleared for Prisma Systems on under FDA product code CDN (Urease, Photometric, Urea Nitrogen). FDA records list 27 510(k) clearances for Prisma Systems, from to . As of , FDA records show no recalls naming K943042.

Clearance record

Decision date
Received
(185 days to decision)
Product code
CDN Urease, Photometric, Urea Nitrogen
Regulation
21 CFR 862.1770
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Prisma Systems 1721 Black River Blvd., Rome NY
510(k) summary
Summary
Third party review
No

Clearances, product code CDN

Trailing 12 months

FDA records hold no clearances under product code CDN in the trailing twelve months.

FDA records show no clearances under product code CDN in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code CDN, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260