Catalog Number

-

Brand Name

BodyGuard® Microset

Version/Model Number

A100-163XES

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

983eda96-5ab6-4c3c-91bc-561205b6d97f

Public Version Date

July 09, 2020

Public Version Number

4

DI Record Publish Date

August 30, 2016

Package DI Number

B101A100163XES1

Quantity per Package

20

Contains DI Package

B101A100163XES0

Package Discontinue Date

November 04, 2019

Package Status

Not in Commercial Distribution

Package Type

Case