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

Tube, Drainage, Suprapubic

21 CFR 876.5090 / Gastroenterology, Urology
FDA source (opens on fda.gov)

FFA is the FDA product code for Tube, Drainage, Suprapubic, a class II device type, regulated under 21 CFR 876.5090. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and 10 recalls.

Classification record

Product code
FFA
Device name
Tube, Drainage, Suprapubic
Regulation
21 CFR 876.5090
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
Yes
Ingested clearances
3
Ingested recalls
10

Clearances, product code FFA

By decision year
3 clearances under product code FFA with a decision year between 1983 and 1994, 1983 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code FFA by decision year
YearClearances
19831
19871
19941

Applicants with the most clearances

Product code FFA
Applicants holding the most 510(k) clearances under product code FFA
ApplicantClearances
Boston Scientific Corporation1
Concept, Inc.1
New England Surgical Instrument Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code