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
K884125Substantially Equivalent

Bio-Tek Automated Microplate Washer Model El403

Bio-Tek Instruments, Inc., Winooski VT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K884125 is the FDA 510(k) clearance record for BIO-TEK AUTOMATED MICROPLATE WASHER MODEL EL403, a class I device, cleared for Bio-Tek Instruments, Inc. on under FDA product code JTC (Device, Microtiter Diluting/Dispensing). FDA records list 37 510(k) clearances for Bio-Tek Instruments, Inc., from to . As of , FDA records show one recall naming K884125.

Clearance record

Decision date
Received
(63 days to decision)
Product code
JTC Device, Microtiter Diluting/Dispensing
Regulation
21 CFR 866.2500
Device class
Class I
Review panel
Microbiology
Applicant
Bio-Tek Instruments, Inc. Hihgland Park, Winooski VT
Third party review
No

Clearances, product code JTC

Trailing 12 months

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

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