The following data is part of a premarket notification filed by Stanbio Laboratory with the FDA for Dir. Quant. Color. Determ. Serum Creat..
Device ID | K771856 |
510k Number | K771856 |
Device Name: | DIR. QUANT. COLOR. DETERM. SERUM CREAT. |
Classification | Alkaline Picrate, Colorimetry, Creatinine |
Applicant | STANBIO LABORATORY 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | CGX |
CFR Regulation Number | 862.1225 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1977-09-29 |
Decision Date | 1977-11-03 |