The following data is part of a premarket notification filed by Bellco Artifidial Organ Spec., Inc. with the FDA for The Bellco Fistula Needles.
| Device ID | K801632 |
| 510k Number | K801632 |
| Device Name: | THE BELLCO FISTULA NEEDLES |
| Classification | Needle, Fistula |
| Applicant | BELLCO ARTIFIDIAL ORGAN SPEC., INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FIE |
| CFR Regulation Number | 876.5540 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-07-15 |
| Decision Date | 1980-08-04 |