The following data is part of a premarket notification filed by Bio Protech, Inc. with the FDA for Proplate.
| Device ID | K073360 |
| 510k Number | K073360 |
| Device Name: | PROPLATE |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | BIO PROTECH, INC. 1676 VILLAGE GREEN SUITE A Crofton, MD 21114 |
| Contact | E.j. Smith |
| Correspondent | Jeff Rongero UNDERWRITERS LABORATORIES, INC. 12 LABORATORY DR. Research Triangle, NC 27709 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | Yes |
| Combination Product | No |
| Date Received | 2007-11-30 |
| Decision Date | 2007-12-19 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() PROPLATE 88854549 not registered Live/Pending |
Rudram Engineering, Inc. 2020-03-31 |
![]() PROPLATE 88854549 not registered Live/Pending |
Proplate, LLC. 2020-03-31 |
![]() PROPLATE 78243279 2956910 Live/Registered |
Bedford Reinforced Plastics, Inc. 2003-04-29 |
![]() PROPLATE 78040122 2613541 Live/Registered |
Professional Plating, Inc. 2000-12-20 |
![]() PROPLATE 77384325 3519524 Live/Registered |
Grace Bio-Labs., Inc. 2008-01-30 |
![]() PROPLATE 75905830 2489240 Dead/Cancelled |
ADIDAS INTERNATIONAL MARKETING B.V. 2000-01-28 |
![]() PROPLATE 75873145 2489117 Dead/Cancelled |
Dieterich Standard, Inc. 1999-12-16 |
![]() PROPLATE 75490378 not registered Dead/Abandoned |
Deluxe Engraving Company 1998-05-22 |
![]() PROPLATE 72347781 0903322 Dead/Expired |
PROTEX INDUSTRIES, INC. 1970-01-05 |