510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K840366Substantially Equivalent

Cell-Matics Herpes Simplex Virus Detect

Difco Laboratories, Inc., Detroit MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K840366 is the FDA 510(k) clearance record for CELL-MATICS HERPES SIMPLEX VIRUS DETECT, a class I device, cleared for Difco Laboratories, Inc. on under FDA product code KIR (Cells, Animal And Human, Cultured). FDA records list 121 510(k) clearances for Difco Laboratories, Inc., from to . As of , FDA records show no recalls naming K840366.

Clearance record

Decision date
Received
(347 days to decision)
Product code
KIR Cells, Animal And Human, Cultured
Regulation
21 CFR 864.2280
Device class
Class I
Review panel
Hematology
Applicant
Difco Laboratories, Inc. P.O. Box 1058-A, Detroit MI
Third party review
No

Clearances, product code KIR

Trailing 12 months

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

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