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

Ocular Peg

21 CFR 886.3320 / Ophthalmic
FDA source (opens on fda.gov)

MQU is the FDA product code for Ocular Peg, a class II device type, regulated under 21 CFR 886.3320. As of , FDA records hold 4 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
MQU
Device name
Ocular Peg
Regulation
21 CFR 886.3320
Device class
Class II
Review panel
Ophthalmic
Submission type
510(k)
Implant
Yes
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
4
Ingested recalls
1

Clearances, product code MQU

By decision year
4 clearances under product code MQU with a decision year between 1997 and 2000, 1998 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code MQU by decision year
YearClearances
19971
19982
20001

Applicants with the most clearances

Product code MQU
Applicants holding the most 510(k) clearances under product code MQU
ApplicantClearances
Integrated Orbital Implants Inc2
Fci Ophthalmics, Inc.1
Porex Technologies Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code