The following data is part of a premarket notification filed by Harry J. Bosworth Co. with the FDA for Liquid A.
Device ID | K981618 |
510k Number | K981618 |
Device Name: | LIQUID A |
Classification | Cement, Dental |
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 | EMA |
CFR Regulation Number | 872.3275 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-05-06 |
Decision Date | 1998-07-28 |