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
K790239Substantially Equivalent

Phytohaemagglutinin

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

K790239 is the FDA 510(k) clearance record for PHYTOHAEMAGGLUTININ, a class I device, cleared for Pharmacia Fine Chemicals on under FDA product code KIQ (Kit, Culture, Chromosome). FDA records list one 510(k) clearance for Pharmacia Fine Chemicals. As of , FDA records show no recalls naming K790239.

Clearance record

Decision date
Received
(35 days to decision)
Product code
KIQ Kit, Culture, Chromosome
Regulation
21 CFR 864.2260
Device class
Class I
Review panel
Hematology
Applicant
Pharmacia Fine Chemicals 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KIQ

Trailing 12 months

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

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