Product code LMQ— Unknown

NORFOLK MEDICAL PERITONEAL-ACCESS PORT

Classification name: Device, Peritoneal Access, Subcutaneous, Implanted
Device class: Class 3
Advisory panel: Unknown
Total cleared: 1
First cleared: 1986-02-04
Most recent: 1986-02-04

Market context for product code LMQ

FDA has cleared 1 device under product code LMQ, all in 1986, filed by 1 applicant company. 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.

Top applicants under product code LMQ

Norfolk Medical Products, Inc.1 clearance

Recent clearances under product code LMQ

K854593 — NORFOLK MEDICAL PERITONEAL-ACCESS PORTNorfolk Medical Products, Inc.·1986-02-04

Data sourced from openFDA. This site is unofficial and independent of the FDA.