The following data is part of a premarket notification filed by Sherwood Medical Industries with the FDA for Lancer L-ina Buffer, Polymer, Wash Solu.
| Device ID | K792014 |
| 510k Number | K792014 |
| Device Name: | LANCER L-INA BUFFER, POLYMER, WASH SOLU |
| Classification | Nephelometer |
| Applicant | SHERWOOD MEDICAL INDUSTRIES 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JZW |
| CFR Regulation Number | 866.4540 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-10-05 |
| Decision Date | 1979-11-13 |