510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K946101Substantially Equivalent

Emergency/accident Trolley 550

Hogan & Hartson, Washington DC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K946101 is the FDA 510(k) clearance record for EMERGENCY/ACCIDENT TROLLEY 550, a class II device, cleared for Hogan & Hartson on under FDA product code FPO (Stretcher, Wheeled). FDA records list 26 510(k) clearances for Hogan & Hartson, from to . As of , FDA records show no recalls naming K946101.

Clearance record

Decision date
Received
(55 days to decision)
Product code
FPO Stretcher, Wheeled
Regulation
21 CFR 880.6910
Device class
Class II
Review panel
General Hospital
Applicant
Hogan & Hartson 555 Thirteenth St. NW, Washington DC
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