The following data is part of a premarket notification filed by Union Broach, Div. Moyco Industries, Inc. with the FDA for Root Canal Files, Type K.
Device ID | K822621 |
510k Number | K822621 |
Device Name: | ROOT CANAL FILES, TYPE K |
Classification | File, Pulp Canal, Endodontic |
Applicant | UNION BROACH, DIV. MOYCO INDUSTRIES, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
Product Code | EKS |
CFR Regulation Number | 872.4565 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1982-08-30 |
Decision Date | 1982-09-28 |