510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K914309Substantially Equivalent

The Genesis Bed from Hill-Rom, Model 355 Series

Hill-Rom Inc., Batesville TN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K914309 is the FDA 510(k) clearance record for THE GENESIS BED FROM HILL-ROM, MODEL 355 SERIES, a class II device, cleared for Hill-Rom, Inc. on under FDA product code HDD (Table, Obstetrical, Ac-Powered (And Accessories)). FDA records list 38 510(k) clearances for Hill-Rom, Inc., from to . As of , FDA records show no recalls naming K914309.

Clearance record

Decision date
Received
(208 days to decision)
Product code
HDD Table, Obstetrical, Ac-Powered (And Accessories)
Regulation
21 CFR 884.4900
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Hill-Rom, Inc. Hwy. 46, Batesville TN
510(k) summary
Statement
Third party review
No

Clearances, product code HDD

Trailing 12 months

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

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