Product code LKX— Unknown

FDA has cleared 18 devices under product code LKX between 1981 and 2018, filed by 17 applicant companies. No FDA device recalls reference this product code.

• 20181 clearance
• 20121 clearance
• 20081 clearance
• 20051 clearance
• 20011 clearance
• 19982 clearances
• 19951 clearance
• 19921 clearance
• 19911 clearance
• 19881 clearance
• 19863 clearances
• 19851 clearance
• 19822 clearances
• 19811 clearance

• J. & Jp., Inc.2 clearances
• Zewa AG1 clearance
• Technology 20001 clearance
• Privi Medical Pte, Ltd.1 clearance
• Medical Appliance Research Corp.1 clearance
• Luther Medical Products, Inc.1 clearance
• Lil Drug Store Products, Inc.1 clearance
• Kure Swiss Medical AG Corp.1 clearance
• Hpk International, Inc.1 clearance
• Fama Holdings International Corp1 clearance

• K172358 — InstaliefPrivi Medical Pte, Ltd.·2018-01-10
• K113660 — COLD PACK, PLASTIC APPLICATOR (MEDICAL GRADE)-NON-CHEMICALCryotherapy Products, Inc.·2012-05-03
• K072414 — CRYOSTATLil Drug Store Products, Inc.·2008-04-07
• K042564 — HEMOR-RITE CRYOTHERAPHYFama Holdings International Corp·2005-09-30
• K012746 — ICE BATONBehive, Ltd.·2001-11-14
• K981428 — ANU ICECryoptherapy Pain Relief Products, Inc.·1998-07-07
• K973590 — HEMORRELIEF DEVICEA.Stein - Regulatory Affairs Consulting·1998-02-05
• K944874 — ZEROID HEMORRHOIDAL DEVICEMedical Appliance Research Corp.·1995-08-07
• K921189 — THERMA-HZewa AG·1992-08-31
• K905276 — THERMA-HKure Swiss Medical AG Corp.·1991-11-07
• K883984 — HEMORX COLD PACKBio-Dyne, Inc.·1988-12-22
• K862490 — ANU-RXJ. & Jp., Inc.·1986-08-18
• K855150 — HPK-A DEVICE DFOR THE TREATMENT OF HEMORRHOIDSHpk International, Inc.·1986-04-01
• K854569 — HEMOR-ICETechnology 2000·1986-02-05
• K852679 — MULTIPLE(HEMORX) IF APPROVED BY TRADEMARK OFFICEJ. & Jp., Inc.·1985-08-09
• K822649 — DEVICE FOR THE TREATMENT OF HEMORRHOIDSDunmore Corp.·1982-11-03
• K822217 — THERMOTHERAPYLuther Medical Products, Inc.·1982-09-24
• K812567 — RELIEFAmerican Pharmaceutical Co., Inc.·1981-11-10