FDA product code LMQ: Device, Peritoneal Access, Subcutaneous, Implanted
LMQ is the FDA product code for device, peritoneal access, subcutaneous, implanted. It is a Class III device, reviewed by the General Hospital panel. FDA has cleared 1 510(k) submission under LMQ. The average 510(k) review took 78 days (median 78).
Classification
| Field | Value |
|---|---|
| Device name | Device, Peritoneal Access, Subcutaneous, Implanted |
| Device class | Class III |
| Review panel | HO — General Hospital |
| Medical specialty | Unknown |
| Premarket route | Contact FDA |
| Implant | Yes |
Compare with all 510(k) review times · Search every LMQ clearance
Top LMQ applicants
| Applicant | Clearances | Latest |
|---|---|---|
| Norfolk Medical Products, Inc. | 1 | 1986-02-04 |
Most recent LMQ clearances
| 510(k) | Applicant | Device | Decision date | Review days |
|---|---|---|---|---|
| K854593 | Norfolk Medical Products, Inc. | NORFOLK MEDICAL PERITONEAL-ACCESS PORT | 1986-02-04 | 78 |
Recalls for LMQ devices
openFDA lists no recalls for product code LMQ.
Frequently asked questions
What is FDA product code LMQ?
LMQ is the FDA product code for device, peritoneal access, subcutaneous, implanted. It is a Class III device, reviewed by the General Hospital panel.
What device class is LMQ?
Class III. Typical premarket route: Contact FDA.
How long does a 510(k) take for product code LMQ?
Across 1 cleared submissions the average was 78 days from receipt to decision (median 78).
Which companies have the most LMQ clearances?
Norfolk Medical Products, Inc. (1).
Next steps
- Run an FDA pathway report with predicate devices for product code LMQ
- Run a recall and safety report across every LMQ manufacturer
- Watch product code LMQ for new clearances and recalls
Source: openFDA device classification, 510(k), PMA, De Novo and recall data (public domain). Review days run from FDA receipt to decision. Not regulatory advice.
All General Hospital product codes · FDA product code lookup · 510(k) database search · 510(k) review times