Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K060140Substantially Equivalent

Crp-Advance Multi Calibrator Set, Model Se-250

Sekisui Diagnostics P.E.I. Inc., Charlottetown, P.E., CA / Traditional, Substantially Equivalent

K060140 is the FDA 510(k) clearance record for CRP-ADVANCE MULTI CALIBRATOR SET, MODEL SE-250, a class II device, cleared for Diagnostic Chemicals , Ltd. on under FDA product code JIT (Calibrator, Secondary). FDA records list 72 510(k) clearances for Sekisui Diagnostics P.E.I. Inc., from to . As of , FDA records show no recalls naming K060140.

Clearance record

Decision date
Received
(95 days to decision)
Product code
JIT Calibrator, Secondary
Regulation
21 CFR 862.1150
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Diagnostic Chemicals , Ltd. 16 Mccarville St., Charlottetown, P.E., CA
510(k) summary
Statement
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