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

Tube, Feeding

21 CFR 876.5980 / Gastroenterology, Urology
FDA source (opens on fda.gov)

FPD is the FDA product code for Tube, Feeding, a class II device type, regulated under 21 CFR 876.5980. As of , FDA records hold 59 510(k) clearances under this code, the most recent dated , and 24 recalls.

Classification record

Product code
FPD
Device name
Tube, Feeding
Regulation
21 CFR 876.5980
Device class
Class II
Review panel
Gastroenterology, Urology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
59
Ingested recalls
24

Clearances, product code FPD

By decision year
59 clearances under product code FPD with a decision year between 1976 and 2024, 1989 the highest year at 6.
Show the numbers
510(k) clearances under FDA product code FPD by decision year
YearClearances
19761
19771
19782
19811
19851
19861
19871
19896
19906
19914
19925
19931
19941
19951
19961
19972
19981
19991
20021
20061
20071
20084
20094
20104
20112
20121
20132
20191
20241

Applicants with the most clearances

Product code FPD
Applicants holding the most 510(k) clearances under product code FPD
ApplicantClearances
Halyard Health6
Sandoz Nutrition6
Biosearch Medical Products, Inc.2
Boston Scientific Corporation2
Intl. Medical Marketing, Inc.2
Philips North America LLC2
Vygon Corp.2
Abbott Medical1
Baxter Healthcare Corporation1
Canadian Hospital Specialties Ltd.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 39 companies shown, in name order