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

Bassinet, Hospital

21 CFR 880.5145 / General Hospital
FDA source (opens on fda.gov)

NZG is the FDA product code for Bassinet, Hospital, a class II device type, regulated under 21 CFR 880.5145. FDA's definition for this code reads: "Intended for medical purposes designed for the use of a pediatric patient made of all construction materials used in a hospital nursery". As of , FDA records hold no 510(k) clearances under this code and 2 recalls.

Classification record

Product code
NZG
Device name
Bassinet, Hospital
FDA definition
Intended for medical purposes designed for the use of a pediatric patient made of all construction materials used in a hospital nursery.
Regulation
21 CFR 880.5145
Device class
Class II
Review panel
General Hospital
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
2

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 25 companies shown, in name order