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

Selector, Color, Spectacle, Lens, Tint

21 CFR 886.1160 / Ophthalmic
FDA source (opens on fda.gov)

NFD is the FDA product code for Selector, Color, Spectacle, Lens, Tint, a class I device type, regulated under 21 CFR 886.1160. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
NFD
Device name
Selector, Color, Spectacle, Lens, Tint
Regulation
21 CFR 886.1160
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
1
Ingested recalls
0

Clearances, product code NFD

By decision year
1 clearance under product code NFD with a decision year between 2001 and 2001, 2001 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code NFD by decision year
YearClearances
20011

Applicants with the most clearances

Product code NFD
Applicants holding the most 510(k) clearances under product code NFD
ApplicantClearances
Cerium Optical Technologies, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code