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
K960669Substantially Equivalent

Hydragel If, 6 If, 12 If Penta Kits/hydragel If, Double If, 2 If, & 4 If Kits

Morax, Chelsea MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K960669 is the FDA 510(k) clearance record for HYDRAGEL IF, 6 IF, 12 IF PENTA KITS/HYDRAGEL IF, DOUBLE IF, 2 IF, & 4 IF KITS, a class II device, cleared for Morax on under FDA product code CFF (Immunoelectrophoretic, Immunoglobulins, (G, A, M)). FDA records list 11 510(k) clearances for Morax, from to . As of , FDA records show no recalls naming K960669.

Clearance record

Decision date
Received
(143 days to decision)
Product code
CFF Immunoelectrophoretic, Immunoglobulins, (G, A, M)
Regulation
21 CFR 866.5510
Device class
Class II
Review panel
Immunology
Applicant
Morax 13805 Waterloo Rd., Chelsea MI
510(k) summary
Statement
Third party review
No

Clearances, product code CFF

Trailing 12 months

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

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