The following data is part of a premarket notification filed by Sigma Diagnostics, Inc. with the FDA for Infinity Ast Reagent (procedure No. 51).
Device ID | K980666 |
510k Number | K980666 |
Device Name: | INFINITY AST REAGENT (PROCEDURE NO. 51) |
Classification | Nadh Oxidation/nad Reduction, Ast/sgot |
Applicant | SIGMA DIAGNOSTICS, INC. 545 SOUTH EWING AVE. St. Louis, MO 63103 |
Contact | William R Gilbert |
Correspondent | William R Gilbert SIGMA DIAGNOSTICS, INC. 545 SOUTH EWING AVE. St. Louis, MO 63103 |
Product Code | CIT |
CFR Regulation Number | 862.1100 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-02-20 |
Decision Date | 1998-03-20 |
Summary: | summary |