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

Stand, Infusion

21 CFR 880.6990 / General Hospital
FDA source (opens on fda.gov)

FOX is the FDA product code for Stand, Infusion, a class I device type, regulated under 21 CFR 880.6990. As of , FDA records hold 36 510(k) clearances under this code, the most recent dated , and 5 recalls.

Classification record

Product code
FOX
Device name
Stand, Infusion
Regulation
21 CFR 880.6990
Device class
Class I
Review panel
General Hospital
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
36
Ingested recalls
5

Clearances, product code FOX

By decision year
36 clearances under product code FOX with a decision year between 1977 and 1998, 1985 the highest year at 7.
Show the numbers
510(k) clearances under FDA product code FOX by decision year
YearClearances
19771
19823
19857
19862
19873
19886
19891
19902
19911
19932
19954
19962
19971
19981

Applicants with the most clearances

Product code FOX
Applicants holding the most 510(k) clearances under product code FOX
ApplicantClearances
Ferguson Medical3
E.F. Brewer Co.2
Allen Medical Systems, Inc.1
Arthro-Medic, Inc.1
Arthrodyn, Inc.1
Automated IV Systems, Inc.1
Broadwest Corp.1
Cambridge Technologies, Inc.1
Camtec1
Clinton Industries, Inc1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 267 companies shown, in name order