Catalog Number

-

Brand Name

Precision Medical Inc.

Version/Model Number

1MFA Air Series

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

May 19, 2021

Issuing Agency

In GS1

MRI safety Status

MR Conditional

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

-

Product Code

CAX

Product Code Name

Flowmeter, Tube, Thorpe, Back-Pressure Compensated

Public Device Record Key

efd4cb4d-a2e7-4bc4-b54e-6b42c285fc13

Public Version Date

May 20, 2021

Public Version Number

5

DI Record Publish Date

April 11, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-