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

Cannula, Ventricular

21 CFR 882.4060 / Neurology
FDA source (opens on fda.gov)

HCD is the FDA product code for Cannula, Ventricular, a class I device type, regulated under 21 CFR 882.4060. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
HCD
Device name
Cannula, Ventricular
Regulation
21 CFR 882.4060
Device class
Class I
Review panel
Neurology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
3
Ingested recalls
0

Clearances, product code HCD

By decision year
3 clearances under product code HCD with a decision year between 1992 and 2015, 1992 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code HCD by decision year
YearClearances
19921
20111
20151

Applicants with the most clearances

Product code HCD
Applicants holding the most 510(k) clearances under product code HCD
ApplicantClearances
Alcyone Lifesciences, Inc.1
Camino Laboratories, Inc.1
Surgivision, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 20 companies shown, in name order