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

Topographer, Corneal, Ac-Powered

21 CFR 886.1350 / Ophthalmic
FDA source (opens on fda.gov)

MMQ is the FDA product code for Topographer, Corneal, Ac-Powered, a class I device type, regulated under 21 CFR 886.1350. As of , FDA records hold 5 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
MMQ
Device name
Topographer, Corneal, Ac-Powered
Regulation
21 CFR 886.1350
Device class
Class I
Review panel
Ophthalmic
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
5
Ingested recalls
0

Clearances, product code MMQ

By decision year
5 clearances under product code MMQ with a decision year between 1995 and 1998, 1997 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code MMQ by decision year
YearClearances
19951
19961
19972
19981

Applicants with the most clearances

Product code MMQ
Applicants holding the most 510(k) clearances under product code MMQ
ApplicantClearances
Bio-Medical Sciences, Inc.1
Eclipse Ventures1
Euclid Systems Corp.1
Orbtek, Inc.1
Par Vision Systems Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 35 companies shown, in name order