510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K951955Substantially Equivalent

Cardon Physical Therapy Table Model:r40194

Cardon Rehabilitation Products, Inc., Niagara Falls NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K951955 is the FDA 510(k) clearance record for CARDON PHYSICAL THERAPY TABLE MODEL:R40194, a class I device, cleared for Cardon Rehabilitation Products, Inc. on under FDA product code INQ (Table, Powered). FDA records list 16 510(k) clearances for Cardon Rehabilitation Products, Inc., from to . As of , FDA records show no recalls naming K951955.

Clearance record

Decision date
Received
(57 days to decision)
Product code
INQ Table, Powered
Regulation
21 CFR 890.3760
Device class
Class I
Review panel
Physical Medicine
Applicant
Cardon Rehabilitation Products, Inc. 2045 Niagara Falls Blvd.,, Niagara Falls NY
510(k) summary
Summary
Third party review
No

Clearances, product code INQ

Trailing 12 months

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

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