The following data is part of a premarket notification filed by Harry J. Bosworth Co. with the FDA for Lc Composite.
Device ID | K991492 |
510k Number | K991492 |
Device Name: | LC COMPOSITE |
Classification | Handpiece, Air-powered, 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 | EFB |
CFR Regulation Number | 872.4200 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1999-04-28 |
Decision Date | 1999-12-02 |