Catalog Number

-

Brand Name

QUICKGEL MODIFIED APPLICATOR BLADES AND DEEP WELL CUPS

Version/Model Number

552136

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K972274

Product Code

CEF

Product Code Name

ELECTROPHORETIC, PROTEIN FRACTIONATION

Public Device Record Key

3ed1aa44-54c5-4783-b71c-7341a795076e

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

March 17, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-