510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K830893Substantially Equivalent

Acth Ria System-Dsi 2300

Diagnostic Systems Laboratories, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K830893 is the FDA 510(k) clearance record for ACTH RIA SYSTEM-DSI 2300, a class II device, cleared for Diagnostic Systems Laboratories, Inc. on under FDA product code CKG (Radioimmunoassay, Acth). FDA records list 94 510(k) clearances for Diagnostic Systems Laboratories, Inc., from to . As of , FDA records show no recalls naming K830893.

Clearance record

Decision date
Received
(37 days to decision)
Product code
CKG Radioimmunoassay, Acth
Regulation
21 CFR 862.1025
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Diagnostic Systems Laboratories, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code CKG

Trailing 12 months

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

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