510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K090339Substantially Equivalent

Belimed Steam Sterilizer Top 5000, Series 8, Models: 6-0-12 Vs1 and Vs2

Belimed Sauter AG, Charleston SC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K090339 is the FDA 510(k) clearance record for BELIMED STEAM STERILIZER TOP 5000, SERIES 8, MODELS: 6-0-12 VS1 AND VS2, a class II device, cleared for Belimed Sauter AG on under FDA product code FLE (Sterilizer, Steam). FDA records list 3 510(k) clearances for Belimed Sauter AG, from to . As of , FDA records show no recalls naming K090339.

Clearance record

Decision date
Received
(225 days to decision)
Product code
FLE Sterilizer, Steam
Regulation
21 CFR 880.6880
Device class
Class II
Review panel
General Hospital
Applicant
Belimed Sauter AG 2284 Clements Ferry Rd., Charleston SC
510(k) summary
Summary PDF
Third party review
No

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