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
K771714Substantially Equivalent

Slide Stainers Gls 360 & 360-1

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

K771714 is the FDA 510(k) clearance record for SLIDE STAINERS GLS 360 & 360-1, a class I device, cleared for Honeywell, Inc. on under FDA product code KEY (Stainer, Tissue, Automated). FDA records list 69 510(k) clearances for Honeywell, Inc., from to . As of , FDA records show no recalls naming K771714.

Clearance record

Decision date
Received
(23 days to decision)
Product code
KEY Stainer, Tissue, Automated
Regulation
21 CFR 864.3800
Device class
Class I
Review panel
Pathology
Applicant
Honeywell, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KEY

Trailing 12 months

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

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