Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K852260Substantially Equivalent

Quick-Chem Calibration Set

Seragen Diagnostics, Inc., Indianapolis IN / Traditional, Substantially Equivalent

K852260 is the FDA 510(k) clearance record for QUICK-CHEM CALIBRATION SET, a class II device, cleared for Seragen Diagnostics, Inc. on under FDA product code JIW (Calibrator, Surrogate). FDA records list 20 510(k) clearances for Seragen Diagnostics, Inc., from to . As of , FDA records show no recalls naming K852260.

Clearance record

Decision date
Received
(59 days to decision)
Product code
JIW Calibrator, Surrogate
Regulation
21 CFR 862.1150
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Seragen Diagnostics, Inc. P.O. Box 1210, Indianapolis IN
Third party review
No

Clearances, product code JIW

Trailing 12 months

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

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