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
K761137Substantially Equivalent

Microsample Blood Collection Device

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

K761137 is the FDA 510(k) clearance record for MICROSAMPLE BLOOD COLLECTION DEVICE, a class I device, cleared for Ortho Diagnostics, Inc. on under FDA product code GKH (Apparatus, Automated Blood Cell Diluting). FDA records list 24 510(k) clearances for Ortho Diagnostics, Inc., from to . As of , FDA records show no recalls naming K761137.

Clearance record

Decision date
Received
(75 days to decision)
Product code
GKH Apparatus, Automated Blood Cell Diluting
Regulation
21 CFR 864.5240
Device class
Class I
Review panel
Hematology
Applicant
Ortho Diagnostics, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code GKH

Trailing 12 months

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

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