The following data is part of a premarket notification filed by Hyland Therapeutic Div., Travenol Laboratories with the FDA for Nephelometric Solid Turbidity Standard.
| Device ID | K812220 |
| 510k Number | K812220 |
| Device Name: | NEPHELOMETRIC SOLID TURBIDITY STANDARD |
| Classification | Calibrator, Surrogate |
| Applicant | HYLAND THERAPEUTIC DIV., TRAVENOL LABORATORIES 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JIW |
| CFR Regulation Number | 862.1150 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-08-06 |
| Decision Date | 1981-08-18 |