510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K782125Substantially Equivalent

Ria Kit, Kanamycin

Siemens Healthcare Diagnostics Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K782125 is the FDA 510(k) clearance record for RIA KIT, KANAMYCIN, a class II device, cleared for Diagnostic Products Corp. on under FDA product code KJI (Radioimmunoassay, Kanamycin). FDA records list 1,204 510(k) clearances for Siemens Healthcare Diagnostics Inc., from to . As of , FDA records show no recalls naming K782125.

Clearance record

Decision date
Received
(14 days to decision)
Product code
KJI Radioimmunoassay, Kanamycin
Regulation
21 CFR 862.3520
Device class
Class II
Review panel
Clinical Toxicology
Applicant
Diagnostic Products Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KJI

Trailing 12 months

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

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