Product code LLD— General Hospital

FDA has cleared 4 devices under product code LLD between 1984 and 1988, filed by 3 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

• 19881 clearance
• 19871 clearance
• 19861 clearance
• 19841 clearance

• Pharmacia, Inc.2 clearances
• Pharmacia Deltec, Inc.1 clearance
• Burron Medical Products, Inc.1 clearance

• K880072 — PORT-A-CATH IMPLANTABLE DRUG DELIVERY SYSTEMPharmacia Deltec, Inc.·1988-03-29
• K864552 — PORT-A-CATH IMPLANTABLE CATHETER SYSTEMPharmacia, Inc.·1987-03-31
• K862412 — INTESTOPLANTBurron Medical Products, Inc.·1986-11-13
• K832906 — PORT-A-CATH IMPLANTABLE CATHETER SYSPharmacia, Inc.·1984-03-06