The following data is part of a premarket notification filed by Harry J. Bosworth Co. with the FDA for Bosworth Liquid Resin Ii.
| Device ID | K961200 |
| 510k Number | K961200 |
| Device Name: | BOSWORTH LIQUID RESIN II |
| Classification | Resin, Denture, Relining, Repairing, Rebasing |
| Applicant | HARRY J. BOSWORTH CO. 7227 NORTH HAMLIN AVE. Skokie, IL 60076 |
| Contact | Mildred M Goldstein |
| Correspondent | Mildred M Goldstein HARRY J. BOSWORTH CO. 7227 NORTH HAMLIN AVE. Skokie, IL 60076 |
| Product Code | EBI |
| CFR Regulation Number | 872.3760 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-03-27 |
| Decision Date | 1996-05-17 |