The following data is part of a premarket notification filed by Sandare Chemical Co., Inc. with the FDA for Sandare Alkaline Phosphatase Procedure.
Device ID | K844498 |
510k Number | K844498 |
Device Name: | SANDARE ALKALINE PHOSPHATASE PROCEDURE |
Classification | Thymolphthalein Monophosphate, Alkaline Phosphatase Or Isoenzymes |
Applicant | SANDARE CHEMICAL CO., INC. P.O. BOX 3028 Desoto, TX 75115 |
Contact | James L Sanders |
Correspondent | James L Sanders SANDARE CHEMICAL CO., INC. P.O. BOX 3028 Desoto, TX 75115 |
Product Code | CIO |
CFR Regulation Number | 862.1050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1984-11-20 |
Decision Date | 1984-12-10 |