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
K931321Substantially Equivalent

Csd 200/300/400/500 Dynamometer

John Chatillon & Sons, Inc., Greensboro NC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K931321 is the FDA 510(k) clearance record for CSD 200/300/400/500 DYNAMOMETER, a class II device, cleared for John Chatillon & Sons, Inc. on under FDA product code LBB (Dynamometer, Ac-Powered). FDA records list 3 510(k) clearances for John Chatillon & Sons, Inc., from to . As of , FDA records show no recalls naming K931321.

Clearance record

Decision date
Received
(336 days to decision)
Product code
LBB Dynamometer, Ac-Powered
Regulation
21 CFR 888.1240
Device class
Class II
Review panel
Orthopedic
Applicant
John Chatillon & Sons, Inc. P.O. Box 35668, Greensboro NC
510(k) summary
Summary
Third party review
No

Clearances, product code LBB

Trailing 12 months

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

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