510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K840858Substantially Equivalent

Ohio 3300 Infant Warmer System

Ohio Medical Products, Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K840858 is the FDA 510(k) clearance record for OHIO 3300 INFANT WARMER SYSTEM, a class II device, cleared for Ohio Medical Products on under FDA product code FMT (Warmer, Infant Radiant). FDA records list 47 510(k) clearances for Ohio Medical Products, from to . As of , FDA records show one recall naming K840858.

Clearance record

Decision date
Received
(28 days to decision)
Product code
FMT Warmer, Infant Radiant
Regulation
21 CFR 880.5130
Device class
Class II
Review panel
General Hospital
Applicant
Ohio Medical Products 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code FMT

Trailing 12 months

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

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