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

Camera, Cine, Endoscopic, With Audio

21 CFR 878.4160 / General, Plastic Surgery
FDA source (opens on fda.gov)

FTS is the FDA product code for Camera, Cine, Endoscopic, With Audio, a class I device type, regulated under 21 CFR 878.4160. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
FTS
Device name
Camera, Cine, Endoscopic, With Audio
Regulation
21 CFR 878.4160
Device class
Class I
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 FTS

By decision year
2 clearances under product code FTS with a decision year between 1988 and 1988, 1988 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code FTS by decision year
YearClearances
19882

Applicants with the most clearances

Product code FTS
Applicants holding the most 510(k) clearances under product code FTS
ApplicantClearances
Medical Concepts2

Companies listing this code with FDA

Companies whose registered establishments list this code