The following data is part of a premarket notification filed by Gilford Instrument Laboratories, Inc. with the FDA for Sba 300 Clinical Chemistry Analyzer.
Device ID | K823233 |
510k Number | K823233 |
Device Name: | SBA 300 CLINICAL CHEMISTRY ANALYZER |
Classification | Analyzer, Chemistry (sequential Multiple, Continuous Flow) Clinical Use |
Applicant | GILFORD INSTRUMENT LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | JJC |
CFR Regulation Number | 862.2150 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1982-10-29 |
Decision Date | 1982-11-29 |