Duns Number:801895244
Device Description: LifeDop 250 Professional with 2.0 MHz, 3.0 MHz and 5.0 MHz EchoHeart Transvaginal Probes
Catalog Number
-
Brand Name
Summit Doppler
Version/Model Number
C250CP
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
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
-
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
K024197,K024197
Product Code
KNG
Product Code Name
Monitor, Ultrasonic, Fetal
Public Device Record Key
90d589e9-8437-4a17-a9a0-721e70340299
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
July 21, 2016
Package DI Number
60888937010055
Quantity per Package
1
Contains DI Package
00888937010053
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 29 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 1471 |
| 3 | A medical device with high risk that requires premarket approval | 2 |