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

Camera, Television, Microsurgical, Without Audio

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

FWD is the FDA product code for Camera, Television, Microsurgical, Without Audio, a class I device type, regulated under 21 CFR 878.4160. As of , FDA records hold 5 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
FWD
Device name
Camera, Television, Microsurgical, 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
5
Ingested recalls
0

Clearances, product code FWD

By decision year
5 clearances under product code FWD with a decision year between 1986 and 1989, 1986 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code FWD by decision year
YearClearances
19863
19881
19891

Applicants with the most clearances

Product code FWD
Applicants holding the most 510(k) clearances under product code FWD
ApplicantClearances
JEDMED Instrument Company4
Medical Dynamics, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code