510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K830462Substantially Equivalent

Abuscreen Radioummunoassay--Urine

Hoffmann-La Roche, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K830462 is the FDA 510(k) clearance record for ABUSCREEN RADIOUMMUNOASSAY--URINE, a class II device, cleared for Hoffmann-La Roche, Inc. on under FDA product code DOE (Radioimmunoassay, Morphine (125-I), Goat Antibody Ammonium Sulfate Sep.). FDA records list 49 510(k) clearances for Hoffmann-La Roche, Inc., from to . As of , FDA records show no recalls naming K830462.

Clearance record

Decision date
Received
(37 days to decision)
Product code
DOE Radioimmunoassay, Morphine (125-I), Goat Antibody Ammonium Sulfate Sep.
Regulation
21 CFR 862.3640
Device class
Class II
Review panel
Clinical Toxicology
Applicant
Hoffmann-La Roche, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code DOE

Trailing 12 months

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

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