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

Illuminator, Non-Remote

21 CFR 878.4580 / General, Plastic Surgery
FDA source (opens on fda.gov)

FTF is the FDA product code for Illuminator, Non-Remote, a class II device type, regulated under 21 CFR 878.4580. As of , FDA records hold 4 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
FTF
Device name
Illuminator, Non-Remote
Regulation
21 CFR 878.4580
Device class
Class II
Review panel
General, Plastic Surgery
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
4
Ingested recalls
0

Clearances, product code FTF

By decision year
4 clearances under product code FTF with a decision year between 1984 and 2004, 1984 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code FTF by decision year
YearClearances
19843
20041

Applicants with the most clearances

Product code FTF
Applicants holding the most 510(k) clearances under product code FTF
ApplicantClearances
Suncoast Medical Manufacturers, Inc.3
Medical Vision Industries, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code