The following data is part of a premarket notification filed by Sterling Diagnostics, Inc. with the FDA for Serum Potassium Reagent Set.
Device ID | K861713 |
510k Number | K861713 |
Device Name: | SERUM POTASSIUM REAGENT SET |
Classification | Tetraphenyl Borate, Colorimetry, Potassium |
Applicant | STERLING DIAGNOSTICS, INC. 34210 DEQUINDRE RD. Sterling Heights, MI 48077 |
Contact | David Callender |
Correspondent | David Callender STERLING DIAGNOSTICS, INC. 34210 DEQUINDRE RD. Sterling Heights, MI 48077 |
Product Code | CEJ |
CFR Regulation Number | 862.1600 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-05-05 |
Decision Date | 1986-05-23 |