510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K832260Substantially Equivalent

Goat Anti-Human Kappa Affinity

Gelco Diagnostics, Inc., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K832260 is the FDA 510(k) clearance record for GOAT ANTI-HUMAN KAPPA AFFINITY, a class II device, cleared for Gelco Diagnostics, Inc. on under FDA product code DEO (Kappa, Fitc, Antigen, Antiserum, Control). FDA records list 14 510(k) clearances for Gelco Diagnostics, Inc., from to . As of , FDA records show no recalls naming K832260.

Clearance record

Decision date
Received
(123 days to decision)
Product code
DEO Kappa, Fitc, Antigen, Antiserum, Control
Regulation
21 CFR 866.5550
Device class
Class II
Review panel
Immunology
Applicant
Gelco Diagnostics, Inc. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code DEO

Trailing 12 months

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

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