Duns Number:174959692
Device Description: RespSense Capnography Monitor
Catalog Number
-
Brand Name
Nonin
Version/Model Number
LS1R-9R
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
K063752,K063752
Product Code
CCK
Product Code Name
Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase
Public Device Record Key
249e3b03-b7bc-4b12-9021-ee5be75f7a33
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
August 24, 2016
Package DI Number
00849686088359
Quantity per Package
1
Contains DI Package
00849686072204
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Box
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 1 |
2 | A medical device with a moderate to high risk that requires special controls. | 130 |