The following data is part of a premarket notification filed by Corning Medical & Scientific with the FDA for Disposable Syringe Filters.
| Device ID | K840556 |
| 510k Number | K840556 |
| Device Name: | DISPOSABLE SYRINGE FILTERS |
| Classification | Filters, Cell Collection, Tissue Processing |
| Applicant | CORNING MEDICAL & SCIENTIFIC 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KET |
| CFR Regulation Number | 864.3010 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-02-08 |
| Decision Date | 1984-03-05 |