FDA 510(k) Applications Submitted by DYMAX CORP.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K032135 | 07/11/2003 | SITE-RITE IV ULTRASOUND SYSTEM | DYMAX CORP. |
| K993624 | 10/26/1999 | SITE-RITE 3 ULTRASOUND SYSTEM | DYMAX CORP. |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact