The following data is part of a premarket notification filed by Blacklock Medical Products, Inc. with the FDA for Periacryl.
| Device ID | K974097 |
| 510k Number | K974097 |
| Device Name: | PERIACRYL |
| Classification | Cement, Dental |
| Applicant | BLACKLOCK MEDICAL PRODUCTS, INC. 6671 LONDON COURT Delta, CA V4k 4w7 |
| Contact | Don Blacklock |
| Correspondent | Don Blacklock BLACKLOCK MEDICAL PRODUCTS, INC. 6671 LONDON COURT Delta, CA V4k 4w7 |
| Product Code | EMA |
| CFR Regulation Number | 872.3275 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-10-30 |
| Decision Date | 1998-04-09 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() PERIACRYL 75302706 2218296 Live/Registered |
Blacklock Medical Products Inc. 1997-06-03 |