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Product codes
NKW
Product code NKW
Device name
Actuator, Syringe, For Injector, Reprocessed
Medical specialty
Cardiovascular
Device class
2
Regulation number
870.1670
Review panel
CV
Implant
N
Life sustaining/supporting
N
GMP exempt
N
Third party review
Y
Summary malfunction reporting
Eligible
Definition
Reprocessing validation data for this device type must be included in a 510(k) submission. (70 FR 56911, available at https://www.govinfo.gov/content/pkg/FR-2005-09-29/pdf/05-19510.pdf).
Source
FDA openFDA device classification dataset
Related GUDID Devices
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Primary DI, Brand, Company table
Primary DI
Brand
Company
Published
03607503507288
JAZZ FRAME
IMPLANET
2019-09-26