The following data is part of a premarket notification filed by Bel-art Products with the FDA for Centidisc.
| Device ID | K813524 |
| 510k Number | K813524 |
| Device Name: | CENTIDISC |
| Classification | Centrifuges (micro, Ultra, Refrigerated) For Clinical Use |
| Applicant | BEL-ART PRODUCTS 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JQC |
| CFR Regulation Number | 862.2050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-12-16 |
| Decision Date | 1981-12-31 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() CENTIDISC 73369897 1262268 Dead/Cancelled |
Bel-Art Products 1982-06-16 |