The following data is part of a premarket notification filed by Kallestad Laboratories, Inc. with the FDA for Kallestad Antisera To Tobramycin.
| Device ID | K812415 |
| 510k Number | K812415 |
| Device Name: | KALLESTAD ANTISERA TO TOBRAMYCIN |
| Classification | Radioimmunoassay, Tobramycin |
| Applicant | KALLESTAD LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KLB |
| CFR Regulation Number | 862.3900 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-08-31 |
| Decision Date | 1981-09-09 |