510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K050374Substantially Equivalent

Advia Ims Lithium Assay

Medrad, Inc., Tarrytown NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K050374 is the FDA 510(k) clearance record for ADVIA IMS LITHIUM ASSAY, a class II device, cleared for Bayer Healthcare, LLC on under FDA product code NDW (Assay, Porphyrin, Spectrophotometry, Lithium). FDA records list 177 510(k) clearances for Medrad, Inc., from to . As of , FDA records show 6 recalls naming K050374.

Clearance record

Decision date
Received
(121 days to decision)
Product code
NDW Assay, Porphyrin, Spectrophotometry, Lithium
Regulation
21 CFR 862.3560
Device class
Class II
Review panel
Clinical Toxicology
Applicant
Bayer Healthcare, LLC 511 Benedict Ave., Tarrytown NY
510(k) summary
Summary PDF
Third party review
No

Clearances, product code NDW

Trailing 12 months

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

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