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

Cannula, Injection

21 CFR 878.4200 / General, Plastic Surgery
FDA source (opens on fda.gov)

FGY is the FDA product code for Cannula, Injection, a class I device type, regulated under 21 CFR 878.4200. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and 7 recalls.

Classification record

Product code
FGY
Device name
Cannula, Injection
Regulation
21 CFR 878.4200
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
7

Clearances, product code FGY

By decision year
2 clearances under product code FGY with a decision year between 1976 and 1982, 1976 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code FGY by decision year
YearClearances
19761
19821

Applicants with the most clearances

Product code FGY
Applicants holding the most 510(k) clearances under product code FGY
ApplicantClearances
B. Braun Instruments1
Kelleher Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 74 companies shown, in name order