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 |