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
K802177Substantially Equivalent

Goat Anti-Human Igm

Protos Laboratories, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K802177 is the FDA 510(k) clearance record for GOAT ANTI-HUMAN IGM, a class II device, cleared for Protos Laboratories on under FDA product code DFT (Igm, Antigen, Antiserum, Control). FDA records list 6 510(k) clearances for Protos Laboratories, from to . As of , FDA records show no recalls naming K802177.

Clearance record

Decision date
Received
(52 days to decision)
Product code
DFT Igm, Antigen, Antiserum, Control
Regulation
21 CFR 866.5550
Device class
Class II
Review panel
Immunology
Applicant
Protos Laboratories 803 N. Front St. Suite 3, Mchenry IL
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