The following data is part of a premarket notification filed by Medical Analysis Systems, Inc. with the FDA for Glucose Hexokinase, Auto K.
| Device ID | K781723 |
| 510k Number | K781723 |
| Device Name: | GLUCOSE HEXOKINASE, AUTO K |
| Classification | Hexokinase, Glucose |
| Applicant | MEDICAL ANALYSIS SYSTEMS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CFR |
| CFR Regulation Number | 862.1345 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-10-11 |
| Decision Date | 1978-11-03 |