Catalog Number

212-080

Brand Name

Aveta Controller

Version/Model Number

212-080

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Unsafe

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

-

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

K190372

Product Code

HIG

Product Code Name

Insufflator, Hysteroscopic

Public Device Record Key

9130dfa2-20d0-4f0d-8f6e-39f533ee6549

Public Version Date

December 04, 2019

Public Version Number

1

DI Record Publish Date

November 26, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-