Catalog Number

-

Brand Name

EACU, EAKU, JOCU, ZAGU

Version/Model Number

NKJ3075

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K150903,K150903,K150903

Product Code

MQX

Product Code Name

Needle, Acupuncture, Single Use

Public Device Record Key

c065c2e2-5ec7-4085-ad41-b4d6af166924

Public Version Date

August 20, 2018

Public Version Number

1

DI Record Publish Date

July 20, 2018

Package DI Number

B338NKJ30752

Quantity per Package

10

Contains DI Package

B338NKJ30751

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

bigger box