510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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LMQClass III

Device, Peritoneal Access, Subcutaneous, Implanted

Unknown
FDA source (opens on fda.gov)

LMQ is the FDA product code for Device, Peritoneal Access, Subcutaneous, Implanted, a class III device type. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
LMQ
Device name
Device, Peritoneal Access, Subcutaneous, Implanted
Device class
Class III
Review panel
Unknown
Submission type
Contact ODE
Implant
Yes
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code LMQ

By decision year
1 clearance under product code LMQ with a decision year between 1986 and 1986, 1986 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code LMQ by decision year
YearClearances
19861

Applicants with the most clearances

Product code LMQ
Applicants holding the most 510(k) clearances under product code LMQ
ApplicantClearances
Norfolk Medical Products, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code LMQ.