The following data is part of a premarket notification filed by Ackrad Laboratories with the FDA for Ackrad V/cug Voiding Cystourethrography Set.
| Device ID | K874293 |
| 510k Number | K874293 |
| Device Name: | ACKRAD V/CUG VOIDING CYSTOURETHROGRAPHY SET |
| Classification | Catheter, Urological |
| Applicant | ACKRAD LABORATORIES 70 JACKSON DR. Cranford, NJ 07016 |
| Contact | Bernard Ackerman |
| Correspondent | Bernard Ackerman ACKRAD LABORATORIES 70 JACKSON DR. Cranford, NJ 07016 |
| Product Code | KOD |
| CFR Regulation Number | 876.5130 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-10-20 |
| Decision Date | 1987-12-29 |