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

Tubing, Dialysate

21 CFR 876.5820 / Gastroenterology, Urology
FDA source (opens on fda.gov)

FID is the FDA product code for Tubing, Dialysate, a class II device type, regulated under 21 CFR 876.5820. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
FID
Device name
Tubing, Dialysate
Regulation
21 CFR 876.5820
Device class
Class II
Review panel
Gastroenterology, Urology
Submission type
510(k)
Implant
No
Life sustaining or supporting
Yes
GMP exempt
No
Third party review eligible
No
Ingested clearances
3
Ingested recalls
0

Clearances, product code FID

By decision year
3 clearances under product code FID with a decision year between 1977 and 2002, 1977 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code FID by decision year
YearClearances
19771
20011
20021

Applicants with the most clearances

Product code FID
Applicants holding the most 510(k) clearances under product code FID
ApplicantClearances
Molded Products Inc2
Norton Performance Plastics Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code