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
K884147Substantially Equivalent

Immunochemical Determination of Immunoglobulin M

Orion Diagnostica, Inc., 02101 Espoo, FI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K884147 is the FDA 510(k) clearance record for IMMUNOCHEMICAL DETERMINATION OF IMMUNOGLOBULIN M, a class II device, cleared for Orion Diagnostica, Inc. on under FDA product code DFT (Igm, Antigen, Antiserum, Control). FDA records list 32 510(k) clearances for Orion Diagnostica, Inc., from to . As of , FDA records show no recalls naming K884147.

Clearance record

Decision date
Received
(24 days to decision)
Product code
DFT Igm, Antigen, Antiserum, Control
Regulation
21 CFR 866.5550
Device class
Class II
Review panel
Immunology
Applicant
Orion Diagnostica, Inc. P.O. Box 83, 02101 Espoo, FI
Third party review
No

Clearances, product code DFT

Trailing 12 months

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

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