510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K850314Substantially Equivalent

Television Control Option 1220

Rehab Technology, Inc., Aviston IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K850314 is the FDA 510(k) clearance record for TELEVISION CONTROL OPTION 1220, a class II device, cleared for Rehab Technology, Inc. on under FDA product code IQA (System, Environmental Control, Powered). FDA records list 4 510(k) clearances for Rehab Technology, Inc., from to . As of , FDA records show no recalls naming K850314.

Clearance record

Decision date
Received
(90 days to decision)
Product code
IQA System, Environmental Control, Powered
Regulation
21 CFR 890.3725
Device class
Class II
Review panel
Physical Medicine
Applicant
Rehab Technology, Inc. Box 185, Aviston IL
Third party review
No

Clearances, product code IQA

Trailing 12 months

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

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