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

Guide And Positioner, Ophthalmic Drug Delivery Device

21 CFR 886.4300 / Ophthalmic
FDA source (opens on fda.gov)

QQQ is the FDA product code for Guide And Positioner, Ophthalmic Drug Delivery Device, a class I device type, regulated under 21 CFR 886.4300. FDA's definition for this code reads: "To provide a guide and/or positioner for filling of a drug delivery device". As of , FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code
QQQ
Device name
Guide And Positioner, Ophthalmic Drug Delivery Device
FDA definition
To provide a guide and/or positioner for filling of a drug delivery device.
Regulation
21 CFR 886.4300
Device class
Class I
Review panel
Ophthalmic
Submission type
Contact ODE
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
0

Companies listing this code with FDA

Companies whose registered establishments list this code

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