510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K865012Substantially Equivalent

Ysi Model 801

Yellow Springs Instrument Co., Inc., Yellow Springs OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K865012 is the FDA 510(k) clearance record for YSI MODEL 801, a class II device, cleared for Yellow Springs Instrument Co., Inc. on under FDA product code FMT (Warmer, Infant Radiant). FDA records list 23 510(k) clearances for Yellow Springs Instrument Co., Inc., from to . As of , FDA records show no recalls naming K865012.

Clearance record

Decision date
Received
(71 days to decision)
Product code
FMT Warmer, Infant Radiant
Regulation
21 CFR 880.5130
Device class
Class II
Review panel
General Hospital
Applicant
Yellow Springs Instrument Co., Inc. 1725 Brannum Ln., Yellow Springs OH
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