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

Gases Used Within Eye To Place Pressure On Detached Retina

21 CFR 886.4270 / Ophthalmic
FDA source (opens on fda.gov)

LPO is the FDA product code for Gases Used Within Eye To Place Pressure On Detached Retina, a class III device type, regulated under 21 CFR 886.4270. As of , FDA records hold no 510(k) clearances under this code and one recall.

Classification record

Product code
LPO
Device name
Gases Used Within Eye To Place Pressure On Detached Retina
Regulation
21 CFR 886.4270
Device class
Class III
Review panel
Ophthalmic
Submission type
PMA
Implant
No
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