510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K810203Substantially Equivalent

Model Am 722

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

K810203 is the FDA 510(k) clearance record for MODEL AM 722, a class II device, cleared for Applied Medical Technologies on under FDA product code JFP (Electrode, Ion Specific, Calcium). FDA records list 24 510(k) clearances for Applied Medical Technologies, from to . As of , FDA records show no recalls naming K810203.

Clearance record

Decision date
Received
(18 days to decision)
Product code
JFP Electrode, Ion Specific, Calcium
Regulation
21 CFR 862.1145
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Applied Medical Technologies 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code JFP

Trailing 12 months

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

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