The following data is part of a premarket notification filed by Biodynamic Technologies, Inc. with the FDA for Cementrifuge.
| Device ID | K851205 |
| 510k Number | K851205 |
| Device Name: | CEMENTRIFUGE |
| Classification | Mixer, Cement, For Clinical Use |
| Applicant | BIODYNAMIC TECHNOLOGIES, INC. 727 TWENTY-THIRD ST. SOUTH Arlington, VA 22202 |
| Contact | Brewster B Taylor |
| Correspondent | Brewster B Taylor BIODYNAMIC TECHNOLOGIES, INC. 727 TWENTY-THIRD ST. SOUTH Arlington, VA 22202 |
| Product Code | JDZ |
| CFR Regulation Number | 888.4210 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-03-26 |
| Decision Date | 1985-07-16 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() CEMENTRIFUGE 73518787 1352467 Dead/Cancelled |
BIODYNAMIC TECHNOLOGIES, INC. 1985-01-23 |