FDA 510(k) Applications for Medical Device Product Code "KRI"
|
FDA 510(k) Number | Applicant | Device Name | Decision Date |
K020365 | 3T MEDICAL SYSTEMS, LLC. | 3TM MYOCARDIAL NEEDLE-TEMPERATURE PROBE | 05/03/2002 |
K992635 | STOECKERT INSTRUMENTE | INTERFACE MODULE IDDD | 12/20/1999 |
K990512 | STOECKERT INSTRUMENTE | STOCKERT POWER SUPPLY UNIT FOR S3 COMPONENTS | 11/23/1999 |