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

Port & Catheter, Implanted, Subcutaneous, Intraperitoneal

21 CFR 880.5965 / General Hospital
FDA source (opens on fda.gov)

LLD is the FDA product code for Port & Catheter, Implanted, Subcutaneous, Intraperitoneal, a class II device type, regulated under 21 CFR 880.5965. As of , FDA records hold 4 510(k) clearances under this code, the most recent dated , and 6 recalls.

Classification record

Product code
LLD
Device name
Port & Catheter, Implanted, Subcutaneous, Intraperitoneal
Regulation
21 CFR 880.5965
Device class
Class II
Review panel
General Hospital
Submission type
510(k)
Implant
Yes
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
4
Ingested recalls
6

Clearances, product code LLD

By decision year
4 clearances under product code LLD with a decision year between 1984 and 1988, 1984 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code LLD by decision year
YearClearances
19841
19861
19871
19881

Applicants with the most clearances

Product code LLD
Applicants holding the most 510(k) clearances under product code LLD
ApplicantClearances
Pharmacia, Inc.2
Burron Medical Products, Inc.1
Pharmacia Deltec, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code