Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K122774Substantially Equivalent

Sakura Steam Sterilizaer Model Assv-Ah06; Sakura Steam Sterilizer Model Assv-Ah06e; Skytron Integrity 175; Skytron Integ

Sakura Seiki Co., Ltd., Chikuma, Nagano, JP / Traditional, Substantially Equivalent

K122774 is the FDA 510(k) clearance record for SAKURA STEAM STERILIZAER MODEL ASSV-AH06; SAKURA STEAM STERILIZER MODEL ASSV-AH06E; SKYTRON INTEGRITY 175; SKYTRON INTEG, a class II device, cleared for Sakura Seiki Co., Ltd. on under FDA product code FLE (Sterilizer, Steam). FDA records list 3 510(k) clearances for Sakura Seiki Co., Ltd., from to . As of , FDA records show no recalls naming K122774.

Clearance record

Decision date
Received
(241 days to decision)
Product code
FLE Sterilizer, Steam
Regulation
21 CFR 880.6880
Device class
Class II
Review panel
General Hospital
Applicant
Sakura Seiki Co., Ltd. 46-1, Shinden, Chikuma, Nagano, JP
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