The following data is part of a premarket notification filed by Sclavo, Inc. with the FDA for Salicylate Test.
Device ID | K843180 |
510k Number | K843180 |
Device Name: | SALICYLATE TEST |
Classification | Colorimetry, Salicylate |
Applicant | SCLAVO, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | DKJ |
CFR Regulation Number | 862.3830 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1984-08-13 |
Decision Date | 1984-09-07 |