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

Implanted Fecal Incontinence Device

Unknown
FDA source (opens on fda.gov)

MIP is the FDA product code for Implanted Fecal Incontinence Device, a class III device type. FDA's definition for this code reads: "PMA Approved: P010020". As of , FDA records hold no 510(k) clearances under this code and one recall.

Classification record

Product code
MIP
Device name
Implanted Fecal Incontinence Device
FDA definition
PMA Approved: P010020
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
1

Companies listing this code with FDA

Companies whose registered establishments list this code