510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K821514Substantially Equivalent

Technicon Ra-1000 Sys, Analytes III

Technicon Instruments Corp., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K821514 is the FDA 510(k) clearance record for TECHNICON RA-1000 SYS, ANALYTES III, a class II device, cleared for Technicon Instruments Corp. on under FDA product code JEJ (Tubing, Instrumentation, Bronchoscope (Brush Sheath A/O Aspirating)). FDA's definition for product code JEJ reads: "If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (82 FR 26807, available at...". FDA records list 157 510(k) clearances for Technicon Instruments Corp., from to . As of , FDA records show no recalls naming K821514.

Clearance record

Decision date
Received
(0 days to decision)
Product code
JEJ Tubing, Instrumentation, Bronchoscope (Brush Sheath A/O Aspirating)
Regulation
21 CFR 874.4680
Device class
Class II
Review panel
Ear, Nose, Throat
Applicant
Technicon Instruments Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code JEJ

Trailing 12 months

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

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