Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K082817Substantially Equivalent

Primus Steam Sterilizer, Models Pss5-G-1 and Pss5-M

PRIMUS Sterilizer Company LLC, Great Bend KS / Traditional, Substantially Equivalent

K082817 is the FDA 510(k) clearance record for PRIMUS STEAM STERILIZER, MODELS PSS5-G-1 AND PSS5-M, a class II device, cleared for Primus Sterilizer Company, LLC on under FDA product code FLE (Sterilizer, Steam). FDA records list 6 510(k) clearances for Primus Sterilizer Company, LLC, from to . As of , FDA records show no recalls naming K082817.

Clearance record

Decision date
Received
(238 days to decision)
Product code
FLE Sterilizer, Steam
Regulation
21 CFR 880.6880
Device class
Class II
Review panel
General Hospital
Applicant
Primus Sterilizer Company, LLC 5520 10th St., Great Bend KS
510(k) summary
Summary PDF
Third party review
Yes

Clearances, product code FLE

Trailing 12 months
4 clearances under product code FLE in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code FLE, trailing twelve months
MonthClearances
November 20250
December 20251
January 20261
February 20261
March 20260
April 20260
May 20260
June 20261
July 20260
August 20260
September 20260
October 20260