The following data is part of a premarket notification filed by Austin Biological Laboratories with the FDA for Spectrum-10.
| Device ID | K831672 |
| 510k Number | K831672 |
| Device Name: | SPECTRUM-10 |
| Classification | Kit, Identification, Enterobacteriaceae |
| Applicant | AUSTIN BIOLOGICAL LABORATORIES 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JSS |
| CFR Regulation Number | 866.2660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-05-23 |
| Decision Date | 1983-06-22 |