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

Lamp, Endoscope, Incandescent

21 CFR 876.1500 / Gastroenterology, Urology
FDA source (opens on fda.gov)

FTI is the FDA product code for Lamp, Endoscope, Incandescent, a class II device type, regulated under 21 CFR 876.1500. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
FTI
Device name
Lamp, Endoscope, Incandescent
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
2
Ingested recalls
0

Clearances, product code FTI

By decision year
2 clearances under product code FTI with a decision year between 1992 and 1997, 1992 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code FTI by decision year
YearClearances
19921
19971

Applicants with the most clearances

Product code FTI
Applicants holding the most 510(k) clearances under product code FTI
ApplicantClearances
Clarus Medical Systems, Inc.1
Dia-Stron, Ltd.1

Companies listing this code with FDA

Companies whose registered establishments list this code