Catalog Number

-

Brand Name

BodyGuard® Microset

Version/Model Number

A120-161XPS

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

November 04, 2019

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"

Yes

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K042696,K042696

Product Code

FPA

Product Code Name

Set, Administration, Intravascular

Public Device Record Key

63762bf6-4677-42e1-8955-f1446ef249a6

Public Version Date

July 09, 2020

Public Version Number

4

DI Record Publish Date

August 08, 2016

Package DI Number

B101A120161XPS1

Quantity per Package

20

Contains DI Package

B101A120161XPS0

Package Discontinue Date

November 04, 2019

Package Status

Not in Commercial Distribution

Package Type

Case