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

Pump, Infusion, Implanted, Programmable

Unknown
FDA source (opens on fda.gov)

LKK is the FDA product code for Pump, Infusion, Implanted, Programmable, a class III device type. As of , FDA records hold no 510(k) clearances under this code and 132 recalls.

Classification record

Product code
LKK
Device name
Pump, Infusion, Implanted, Programmable
Device class
Class III
Review panel
Unknown
Submission type
PMA
Implant
Yes
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
132

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 19 companies shown, in name order