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 |