Product code LLF— Unknown

FDA has cleared 4 devices under product code LLF between 1984 and 1987, filed by 4 applicant companies. No FDA device recalls reference this product code. Class III devices are high-risk and generally require premarket approval (PMA); 510(k) clearance under a Class III product code is limited to certain preamendments-type devices.

• 19872 clearances
• 19861 clearance
• 19841 clearance

• Inframed, Inc.1 clearance
• Hgm, Inc.1 clearance
• Cooper Medical Corp.1 clearance
• Britt Corp., Inc.1 clearance

• K870773 — ENDOCOAGULATOR MODELS 5, 8 & 20 ARGON LASERHgm, Inc.·1987-07-10
• K864610 — CILAS YM 101 ND:YAG LASER FOR NEUROLOGICAL USEInframed, Inc.·1987-06-18
• K860977 — MODEL 545-45 FOR NEUROLOGICAL SURGICAL APPLICATIONBritt Corp., Inc.·1986-10-16
• K833497 — COOPER MEDICAL MODEL 770Cooper Medical Corp.·1984-04-17