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

Illuminator, Remote

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

FTG is the FDA product code for Illuminator, Remote, a class II device type, regulated under 21 CFR 878.4580. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
FTG
Device name
Illuminator, Remote
Regulation
21 CFR 878.4580
Device class
Class II
Review panel
General, Plastic Surgery
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
2
Ingested recalls
0

Clearances, product code FTG

By decision year
2 clearances under product code FTG with a decision year between 1976 and 1980, 1976 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code FTG by decision year
YearClearances
19761
19801

Applicants with the most clearances

Product code FTG
Applicants holding the most 510(k) clearances under product code FTG
ApplicantClearances
Cobe Laboratories, Inc.1
Int'L Marketing & Sales Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code