510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K943969Substantially Equivalent

Model 578 Mobile Surgical Stretcher

Hausted, Inc., Medina OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K943969 is the FDA 510(k) clearance record for MODEL 578 MOBILE SURGICAL STRETCHER, a class II device, cleared for Hausted, Inc. on under FDA product code FPO (Stretcher, Wheeled). FDA records list 2 510(k) clearances for Hausted, Inc. As of , FDA records show no recalls naming K943969.

Clearance record

Decision date
Received
(163 days to decision)
Product code
FPO Stretcher, Wheeled
Regulation
21 CFR 880.6910
Device class
Class II
Review panel
General Hospital
Applicant
Hausted, Inc. 927 Lake Rd., Medina OH
510(k) summary
Summary
Third party review
No

Clearances, product code FPO

Trailing 12 months

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

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