The following data is part of a premarket notification filed by Pentron Corp. with the FDA for Number 20 R/l System.
Device ID | K841458 |
510k Number | K841458 |
Device Name: | NUMBER 20 R/L SYSTEM |
Classification | Agent, Tooth Bonding, Resin |
Applicant | PENTRON CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | KLE |
CFR Regulation Number | 872.3200 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1984-04-09 |
Decision Date | 1984-05-22 |