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

Photorefractor

21 CFR 886.1120 / Ophthalmic
FDA source (opens on fda.gov)

MMF is the FDA product code for Photorefractor, a class II device type, regulated under 21 CFR 886.1120. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
MMF
Device name
Photorefractor
Regulation
21 CFR 886.1120
Device class
Class II
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
1
Ingested recalls
0

Clearances, product code MMF

By decision year
1 clearance under product code MMF with a decision year between 1994 and 1994, 1994 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code MMF by decision year
YearClearances
19941

Applicants with the most clearances

Product code MMF
Applicants holding the most 510(k) clearances under product code MMF
ApplicantClearances
Medical Technology and Innovations, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code