The following data is part of a premarket notification filed by Sigma Diagnostics, Inc. with the FDA for Sigma Diagnostics Wash Concentrate.
Device ID | K963539 |
510k Number | K963539 |
Device Name: | SIGMA DIAGNOSTICS WASH CONCENTRATE |
Classification | Analyzer, Chemistry (photometric, Discrete), For Clinical Use |
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 | JJE |
Subsequent Product Code | CDS |
Subsequent Product Code | CEM |
Subsequent Product Code | CGA |
Subsequent Product Code | CGZ |
Subsequent Product Code | JFP |
Subsequent Product Code | JGS |
Subsequent Product Code | KHS |
CFR Regulation Number | 862.2160 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-09-04 |
Decision Date | 1996-12-16 |
Summary: | summary |