The following data is part of a premarket notification filed by Beiersdorf, Inc. with the FDA for Norta Siliconized Latex Balloon Cath..
| Device ID | K842420 |
| 510k Number | K842420 |
| Device Name: | NORTA SILICONIZED LATEX BALLOON CATH. |
| Classification | Catheter, Urological |
| Applicant | BEIERSDORF, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Contact | John R Trembley |
| Correspondent | John R Trembley BEIERSDORF, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KOD |
| CFR Regulation Number | 876.5130 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-06-20 |
| Decision Date | 1984-11-21 |