510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K900307Substantially Equivalent

Kare Chair I

Kare Chair Industries, Inc., Findley MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K900307 is the FDA 510(k) clearance record for KARE CHAIR I, a class II device, cleared for Kare Chair Industries, Inc. on under FDA product code INO (Chair, Positioning, Electric). FDA records list one 510(k) clearance for Kare Chair Industries, Inc. As of , FDA records show no recalls naming K900307.

Clearance record

Decision date
Received
(25 days to decision)
Product code
INO Chair, Positioning, Electric
Regulation
21 CFR 890.3110
Device class
Class II
Review panel
Physical Medicine
Applicant
Kare Chair Industries, Inc. 6470 Riverview Ter., Findley MN
Third party review
No

Clearances, product code INO

Trailing 12 months

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

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