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

Device, Storage, Images, Ophthalmic

21 CFR 892.2010 / Radiology
FDA source (opens on fda.gov)

NFF is the FDA product code for Device, Storage, Images, Ophthalmic, a class I device type, regulated under 21 CFR 892.2010. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and one recall.

Classification record

Product code
NFF
Device name
Device, Storage, Images, Ophthalmic
Regulation
21 CFR 892.2010
Device class
Class I
Review panel
Radiology
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
1

Clearances, product code NFF

By decision year
1 clearance under product code NFF with a decision year between 2002 and 2002, 2002 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code NFF by decision year
YearClearances
20021

Applicants with the most clearances

Product code NFF
Applicants holding the most 510(k) clearances under product code NFF
ApplicantClearances
Carl Zeiss Meditec Inc1

Companies listing this code with FDA

Companies whose registered establishments list this code