510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K871012Substantially Equivalent

Continuous Passive Motion Patient Kit or Re. Pad

Cropper Medical, Inc., Ashland OR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K871012 is the FDA 510(k) clearance record for CONTINUOUS PASSIVE MOTION PATIENT KIT OR RE. PAD, a class I device, cleared for Cropper Medical, Inc. on under FDA product code BXB (Exerciser, Powered). FDA records list 2 510(k) clearances for Cropper Medical, Inc., from to . As of , FDA records show no recalls naming K871012.

Clearance record

Decision date
Received
(12 days to decision)
Product code
BXB Exerciser, Powered
Regulation
21 CFR 890.5380
Device class
Class I
Review panel
Physical Medicine
Applicant
Cropper Medical, Inc. 330 Hershey St., Ashland OR
Third party review
No

Clearances, product code BXB

Trailing 12 months

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

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