510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K952725Substantially Equivalent

Multicheck

Radiometer America, Inc, Westlake OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K952725 is the FDA 510(k) clearance record for MULTICHECK, a class II device, cleared for Radiometer America, Inc. on under FDA product code GLY (Oximeter To Measure Hemoglobin). FDA records list 50 510(k) clearances for Radiometer America, Inc., from to . As of , FDA records show no recalls naming K952725.

Clearance record

Decision date
Received
(251 days to decision)
Product code
GLY Oximeter To Measure Hemoglobin
Regulation
21 CFR 864.7500
Device class
Class II
Review panel
Hematology
Applicant
Radiometer America, Inc. 810 Sharon Dr., Westlake OH
510(k) summary
Summary
Third party review
No

Clearances, product code GLY

Trailing 12 months

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

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