510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K063705Substantially Equivalent

Lithium Micro Volume Electrode, Theophylline, Ise Calibrators 1, 2 and 3, Tdm Calibration Set B, Nortrol and Abtrol

Thermo Electron Oy, Vantaa, FI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K063705 is the FDA 510(k) clearance record for LITHIUM MICRO VOLUME ELECTRODE, THEOPHYLLINE, ISE CALIBRATORS 1, 2 AND 3, TDM CALIBRATION SET B, NORTROL AND ABTROL, a class II device, cleared for Thermo Electron OY on under FDA product code NDW (Assay, Porphyrin, Spectrophotometry, Lithium). FDA records list 14 510(k) clearances for Thermo Electron OY, from to . As of , FDA records show no recalls naming K063705.

Clearance record

Decision date
Received
(300 days to decision)
Product code
NDW Assay, Porphyrin, Spectrophotometry, Lithium
Regulation
21 CFR 862.3560
Device class
Class II
Review panel
Clinical Toxicology
Applicant
Thermo Electron OY Ratastie 2, Vantaa, FI
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