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 |