FDA 510(k) Applications Submitted by HANS BIOMED CORP.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K151271 | 05/13/2015 | BellaFuse | Hans Biomed Corp. |
| K152077 | 07/27/2015 | MaxiGen | HANS BIOMED CORP. |
| K113728 | 12/19/2011 | SURFUSE GEL AND PUTTY, EXFUSE GEL AND PUTTY | HANS BIOMED CORP. |
| K130235 | 01/30/2013 | SURFUSE II GEL, SURFUSE II PUTTY, EXFUSE II GEL, EXFUSE II PUTTY | HANS BIOMED CORP. |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact