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

Camera, Cine, Endoscopic, Without Audio

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

FWL is the FDA product code for Camera, Cine, Endoscopic, Without 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
FWL
Device name
Camera, Cine, Endoscopic, Without 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 FWL

By decision year
2 clearances under product code FWL with a decision year between 1988 and 1995, 1988 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code FWL by decision year
YearClearances
19881
19951

Applicants with the most clearances

Product code FWL
Applicants holding the most 510(k) clearances under product code FWL
ApplicantClearances
Storz Instrument Co.1
Wells Johnson Co.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 31 companies shown, in name order