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

Catheter, Ventricular (Containing Antibiotic Or Antimicrobial Agents)

21 CFR 882.4100 / Neurology
FDA source (opens on fda.gov)

NHC is the FDA product code for Catheter, Ventricular (Containing Antibiotic Or Antimicrobial Agents), a class II device type, regulated under 21 CFR 882.4100. FDA's definition for this code reads: "Used to gain access to the cavities of the brain for injection of material into or removal of material from the brain". As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and 2 recalls.

Classification record

Product code
NHC
Device name
Catheter, Ventricular (Containing Antibiotic Or Antimicrobial Agents)
FDA definition
Used to gain access to the cavities of the brain for injection of material into or removal of material from the brain.
Regulation
21 CFR 882.4100
Device class
Class II
Review panel
Neurology
Submission type
510(k)
Implant
Yes
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
3
Ingested recalls
2

Clearances, product code NHC

By decision year
3 clearances under product code NHC with a decision year between 2001 and 2016, 2001 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code NHC by decision year
YearClearances
20011
20071
20161

Applicants with the most clearances

Product code NHC
Applicants holding the most 510(k) clearances under product code NHC
ApplicantClearances
Cook Inc.2
Cook Incorporated1

Companies listing this code with FDA

Companies whose registered establishments list this code