510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
NZDClass I

Stretcher, Patient Restraint

21 CFR 880.6900 / General Hospital
FDA source (opens on fda.gov)

NZD is the FDA product code for Stretcher, Patient Restraint, a class I device type, regulated under 21 CFR 880.6900. FDA's definition for this code reads: "Soft restraints to be attached to a backboard or stretcher in order to immobilize the patient in emgency situations". As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and 2 recalls.

Classification record

Product code
NZD
Device name
Stretcher, Patient Restraint
FDA definition
Soft restraints to be attached to a backboard or stretcher in order to immobilize the patient in emgency situations.
Regulation
21 CFR 880.6900
Device class
Class I
Review panel
General Hospital
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
1
Ingested recalls
2

Clearances, product code NZD

By decision year
1 clearance under product code NZD with a decision year between 2006 and 2006, 2006 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code NZD by decision year
YearClearances
20061

Applicants with the most clearances

Product code NZD
Applicants holding the most 510(k) clearances under product code NZD
ApplicantClearances
Emergency Products & Research, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 61 companies shown, in name order