510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K893598Substantially Equivalent

Hydraulic Foot Operated Stool

Arthro-Medic, Inc., Jacksonville FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K893598 is the FDA 510(k) clearance record for HYDRAULIC FOOT OPERATED STOOL, a class I device, cleared for Arthro-Medic, Inc. on under FDA product code GBB (Chair, Surgical, Ac-Powered). FDA records list 4 510(k) clearances for Arthro-Medic, Inc., from to . As of , FDA records show no recalls naming K893598.

Clearance record

Decision date
Received
(154 days to decision)
Product code
GBB Chair, Surgical, Ac-Powered
Regulation
21 CFR 878.4960
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Arthro-Medic, Inc. 4203 Belfort Rd., Suite 150, Jacksonville FL
Third party review
No

Clearances, product code GBB

Trailing 12 months

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

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