510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K090136Substantially Equivalent

Steris Cmax Xlt Surgical Table

STERIS Corporation, Mentor OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K090136 is the FDA 510(k) clearance record for STERIS CMAX XLT SURGICAL TABLE, a class I device, cleared for STERIS Corporation on under FDA product code FQO (Table, Operating-Room, Ac-Powered). FDA records list 227 510(k) clearances for STERIS Corporation, from to . As of , FDA records show 4 recalls naming K090136.

Clearance record

Decision date
Received
(58 days to decision)
Product code
FQO Table, Operating-Room, Ac-Powered
Regulation
21 CFR 878.4960
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
STERIS Corporation 5960 Heisley Rd., Mentor OH
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FQO

Trailing 12 months

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

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