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

Basin, Emesis

21 CFR 880.6730 / General Hospital
FDA source (opens on fda.gov)

FNY is the FDA product code for Basin, Emesis, a class I device type, regulated under 21 CFR 880.6730. As of , FDA records hold 9 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
FNY
Device name
Basin, Emesis
Regulation
21 CFR 880.6730
Device class
Class I
Review panel
General Hospital
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
9
Ingested recalls
1

Clearances, product code FNY

By decision year
9 clearances under product code FNY with a decision year between 1976 and 1984, 1976 the highest year at 4.
Show the numbers
510(k) clearances under FDA product code FNY by decision year
YearClearances
19764
19771
19803
19841

Applicants with the most clearances

Product code FNY
Applicants holding the most 510(k) clearances under product code FNY
ApplicantClearances
Landmark Plastics3
American Hospital Supply1
Bemis Health Care1
Concord Laboratories, Inc.1
Premium Plastics, Inc.1
Procter & Gamble Mfg. Co.1
Texas Medical Products, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 207 companies shown, in name order