510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K841556Substantially Equivalent

Heart - Aid Als, 95

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

K841556 is the FDA 510(k) clearance record for HEART - AID ALS, 95, a class II device, cleared for Cardiac Resucitator Corp. on under FDA product code LDO (Enzymatic Radiochemical Assay, Tobramycin). FDA records list 17 510(k) clearances for Cardiac Resucitator Corp., from to . As of , FDA records show no recalls naming K841556.

Clearance record

Decision date
Received
(94 days to decision)
Product code
LDO Enzymatic Radiochemical Assay, Tobramycin
Regulation
21 CFR 862.3900
Device class
Class II
Review panel
Clinical Toxicology
Applicant
Cardiac Resucitator Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code LDO

Trailing 12 months

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

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