The following data is part of a premarket notification filed by Block Drug Company, Inc. with the FDA for Super Poli-grip & Wernet's Denture Adhes. Powder.
| Device ID | K872225 |
| 510k Number | K872225 |
| Device Name: | SUPER POLI-GRIP & WERNET'S DENTURE ADHES. POWDER |
| Classification | Carboxymethylcellulose Sodium Or Polyvinyl Methylether Maleic Acid Calcium-sodium |
| Applicant | BLOCK DRUG COMPANY, INC. 257 CORNELISON AVE. Jersey City, NJ 07302 |
| Contact | Howard Feinman |
| Correspondent | Howard Feinman BLOCK DRUG COMPANY, INC. 257 CORNELISON AVE. Jersey City, NJ 07302 |
| Product Code | KOT |
| CFR Regulation Number | 872.3490 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-06-09 |
| Decision Date | 1987-06-30 |