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 |