Medical Device
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K222849Substantially Equivalent

AMSCO 600 Steam Sterilizer, V-PRO maX 2 Low Temperature Sterilization System, V-PRO s2 Low Temperature Sterilization System, V-PRO 60 Low Temperature Sterilization System, RAS 12 Rack, RAS 12 Long Rack, RAS Cycle of the AMSCO 7052HP and 7053HP Single Chamber Washer Disinfector

STERIS Corporation, Mentor OH / Special, Substantially Equivalent

K222849 is the FDA 510(k) clearance record for AMSCO 600 Steam Sterilizer, V-PRO maX 2 Low Temperature Sterilization System, V-PRO s2 Low Temperature Sterilization System, V-PRO 60 Low Temperature Sterilization System, RAS 12 Rack, RAS 12 Long Rack, RAS Cycle of the AMSCO 7052HP and 7053HP Single Chamber Washer Disinfector, a class II device, cleared for Steris on under FDA product code NVE (Washer, Cleaner, Automated, Endoscope). FDA's definition for product code NVE reads: "This automated device is intended to be used to clean endoscopes. Endoscopes that are intended to be cleaned by the automated cleaner system should have been pre-cleaned and tested for leaks and lumen obstructions according to the...". FDA records list 227 510(k) clearances for Steris, from to . As of , FDA records show no recalls naming K222849.

Clearance record

Decision date
Received
(9 days to decision)
Product code
NVE Washer, Cleaner, Automated, Endoscope
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Steris 5960 Heisley Rd., Mentor OH
510(k) summary
Summary PDF
Third party review
No

Clearances, product code NVE

Trailing 12 months

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

FDA records show no clearances under product code NVE in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code NVE, 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