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
K810733Substantially Equivalent

Harris Hematoxylin

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

K810733 is the FDA 510(k) clearance record for HARRIS HEMATOXYLIN, a class I device, cleared for Surgipath on under FDA product code HYK (Hematoxylin Harris'S). FDA records list 12 510(k) clearances for Surgipath, from to . As of , FDA records show no recalls naming K810733.

Clearance record

Decision date
Received
(27 days to decision)
Product code
HYK Hematoxylin Harris'S
Regulation
21 CFR 864.1850
Device class
Class I
Review panel
Hematology
Applicant
Surgipath 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code HYK

Trailing 12 months

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

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