The following data is part of a premarket notification filed by Sandare Chemical Co., Inc. with the FDA for Sandare Cyanmethemoglobin Standard.
Device ID | K792358 |
510k Number | K792358 |
Device Name: | SANDARE CYANMETHEMOGLOBIN STANDARD |
Classification | Calibrator For Hemoglobin And Hematocrit Measurement |
Applicant | SANDARE CHEMICAL CO., INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | KRZ |
CFR Regulation Number | 864.8165 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1979-11-21 |
Decision Date | 1979-12-31 |