510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K875280Substantially Equivalent

Steris System 1 Processor and 20 Sterilant

Steris C/O Medical Device Consultants, Inc., North Attleboro MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K875280 is the FDA 510(k) clearance record for STERIS SYSTEM 1 PROCESSOR AND 20 STERILANT, a class II device, cleared for Steris C/O Medical Device Consultants, Inc. on under FDA product code MED (Sterilant, Medical Devices). FDA records list one 510(k) clearance for Steris C/O Medical Device Consultants, Inc. As of , FDA records show 3 recalls naming K875280.

Clearance record

Decision date
Received
(264 days to decision)
Product code
MED Sterilant, Medical Devices
Regulation
21 CFR 880.6885
Device class
Class II
Review panel
General Hospital
Applicant
Steris C/O Medical Device Consultants, Inc. 45 W. St., North Attleboro MA
Third party review
No

Clearances, product code MED

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