510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K921817Substantially Equivalent

Rifton Mor219 19 & Rifton Mor225 25

Rifton Equipment for the Handicapped, Great Neck NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K921817 is the FDA 510(k) clearance record for RIFTON MOR219 19 & RIFTON MOR225 25, a class I device, cleared for Rifton Equipment For the Handicapped on under FDA product code INM (Chair, With Casters). FDA records list 7 510(k) clearances for Rifton Equipment For the Handicapped, from to . As of , FDA records show no recalls naming K921817.

Clearance record

Decision date
Received
(14 days to decision)
Product code
INM Chair, With Casters
Regulation
21 CFR 890.3100
Device class
Class I
Review panel
Physical Medicine
Applicant
Rifton Equipment For the Handicapped 55 Northern Blvd., Great Neck NY
510(k) summary
Statement
Third party review
No

Clearances, product code INM

Trailing 12 months

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

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