The following data is part of a premarket notification filed by Kerr Corporation (danbury) with the FDA for Reflect Impression Material.
Device ID | K781689 |
510k Number | K781689 |
Device Name: | REFLECT IMPRESSION MATERIAL |
Classification | Material, Impression |
Applicant | KERR CORPORATION (DANBURY) 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | ELW |
CFR Regulation Number | 872.3660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1978-10-04 |
Decision Date | 1978-11-15 |