510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K834080Substantially Equivalent

Matched Component Set for Digitoxin

Cambridge Medical Technology, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K834080 is the FDA 510(k) clearance record for MATCHED COMPONENT SET FOR DIGITOXIN, a class II device, cleared for Cambridge Medical Technology on under FDA product code LCW (Radioimmunoassay, Digitoxin (125-I)). FDA records list 14 510(k) clearances for Cambridge Medical Technology, from to . As of , FDA records show no recalls naming K834080.

Clearance record

Decision date
Received
(68 days to decision)
Product code
LCW Radioimmunoassay, Digitoxin (125-I)
Regulation
21 CFR 862.3300
Device class
Class II
Review panel
Clinical Toxicology
Applicant
Cambridge Medical Technology 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code LCW

Trailing 12 months

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

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