510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K141728Substantially Equivalent

Ace Calibrator

Sentinel CH SpA, Milan, IT / Abbreviated, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K141728 is the FDA 510(k) clearance record for ACE CALIBRATOR, a class II device, cleared for SENTINEL CH. SpA on under FDA product code JIT (Calibrator, Secondary). FDA records list 22 510(k) clearances for SENTINEL CH. SpA, from to . As of , FDA records show no recalls naming K141728.

Clearance record

Decision date
Received
(32 days to decision)
Product code
JIT Calibrator, Secondary
Regulation
21 CFR 862.1150
Device class
Class II
Review panel
Clinical Chemistry
Applicant
SENTINEL CH. SpA Via Robert Koch 2, Milan, IT
510(k) summary
Summary PDF
Third party review
No

Clearances, product code JIT

Trailing 12 months

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

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